F 0550
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Honor the resident's right to a dignified existence, self-determination, communication, and to exercise his or
her rights.
Based on observation, interview and records review, the facility failed to protect privacy for one (R101)
resident of six residents reviewed in a sample of 29. R101's current face sheet documents R101's diagnosis
to include but not limited to: unspecified dementia, unspecified severity, without behavioral disturbance,
psychotic disturbance, mood disturbance, and anxiety, alcoholic cirrhosis of liver without ascites, adult
failure to thrive, dysphagia, oropharyngeal phase. R101's Brief Interview for Mental Status (BIMS) dated
08/22/2025 documents R101 has BIMS score of 6/15, indicating R1 has severe cognitive disability. On
09/09/205 at 12:00PM, R101 was observed wearing a wrist band from a nearby hospital on his left wrist
that documented his name, age, gender, date of birth .On 09/09/2025 at 12:02PM, V14 (Registered
Nurse-RN) observed R101's wrist band and stated R101 came back with it from a recent hospital visit. V14
stated the wrist band should have been removed when R101got back to the facility because the wrist
exposed R1's personal information; full name, age, date of birth , and gender, and anyone can see the
information on the wrist band. V14 stated this was a HIPAA (Health Insurance Portability and Accountability
Act) violation. On 09/11/2025 at 10:50AM, V2 (Director of Nursing-DON) V2 stated R101 when come back
from the hospital, the wrist band from the hospital should have been removed to protect R101's privacy
because the wrist band showed R101's identifying private information such as date of birth , age, name and
gender and was exposed where anyone could see R101's personal information which is a HIPAA concern.
Policy titled Dignity dated 4-23-18 documents: -Place labels on each resident in a way that is conspicuous
and respects his or her dignity.
Any deficiency statement ending with an asterisk (*) denotes a deficiency which the institution may be excused from correcting providing it is determined that other
safeguards provide sufficient protection to the patients. (See instructions.) Except for nursing homes, the findings stated above are disclosable 90 days following the
date of survey whether or not a plan of correction is provided. For nursing homes, the above findings and plans of correction are disclosable 14 days following the date
these documents are made available to the facility. If deficiencies are cited, an approved plan of correction is requisite to continued program participation.
LABORATORY DIRECTOR'S OR PROVIDER/SUPPLIER
REPRESENTATIVE'S SIGNATURE
TITLE
(X6) DATE
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Facility ID:
If continuation sheet
Page 1 of 20
Event ID:
145867
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
145867
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/12/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Alta Rehab at Fairmont
5061 North Pulaski Road
Chicago, IL 60630
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0554
Allow residents to self-administer drugs if determined clinically appropriate.
Level of Harm - Minimal harm
or potential for actual harm
Based on observation, interview, and record review the facility failed to obtain a physician order, develop
plan of care and determine if self-administration of medication was appropriate for one (R52) of one
resident observed with medication at bed side table in a sample of 29. The findings include:R52's
admission record showed initial admit date on 7/26/2024 with diagnoses not limited to End stage renal
disease, Dependence on renal dialysis, Benign prostatic hyperplasia, Essential (primary) hypertension,
Multiple subsegmental thrombotic pulmonary emboli, Unspecified atrial fibrillation, Obstructive and reflux
uropathy, Wedge compression fracture of fourth lumbar vertebra, Wedge compression fracture of second
lumbar vertebra. MDS (Minimum Data Set) dated 8/6/2025 showed R52's cognition was intact. On 9/9/25 at
12:36 PM Observed R52 resting in bed, alert and verbally responsive. Appears comfortable and well
groomed. Observed 2 brown with green capsules in the medication cup at bedside. R52 said it was brought
by the nurse, not sure when. On 9/9/25 At 12:39PM Surveyor requested V28 (Licensed Practical Nurse /
LPN) to R52's room and stated those 2 capsules are Tamsulosin / Flomax and it is scheduled at nighttime.
Stated maybe the night nurse left it at bedside. On 9/11/25 At 9:18AM V2 (Director of Nursing / DON) stated
nurses are not supposed to keep or leave medications at bedside. She said self-medication administration
should be determined or assessed to determine if the resident is able /can safely self-administer
medication and if they are cognitively appropriate to keep medication at bedside. V2 said self-administration
should have a physician order and should be care planned. V2 stated if medications were left at bedside,
the nurse would not know the exact time the resident took the medications, and not following medication
timing of physician order and resident could possibly result in not receiving the therapeutic effect of the
medication. R52's electronic health record reviewed with V2 and did not find assessment and care plan for
self-administration and no physician order for medication to leave at bedside. R52's POS (Physician order
sheet) dated 9/9/25 and MAR (Medication Administration Record) showed active order not limited to
Tamsulosin HCl Oral Capsule 0.4 MG Give 2 capsule by mouth at bedtime at 9PM related to Benign
Prostatic Hyperplasia. Facility's Self-administration of medications policy dated 8/2020 showed in part: In
order to maintain the residents' high level of independence, residents who desire to self-administer
medications are permitted to do so if the facility's interdisciplinary team (or equivalent) has determined that
the practice would be safe for the resident and other residents of the facility and there is a prescriber's
order to self- administer. If the resident desires to self-administer medications, an assessment is conducted
by the interdisciplinary team of the resident's cognitive, physical and visual ability to carry out this
responsibility during the care planning process.
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145867
If continuation sheet
Page 2 of 20
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
145867
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/12/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Alta Rehab at Fairmont
5061 North Pulaski Road
Chicago, IL 60630
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0638
Assure that each resident’s assessment is updated at least once every 3 months.
Level of Harm - Minimal harm
or potential for actual harm
Based on interview and record review, the facility failed to complete the Quarterly Minimum Data Set (MDS)
assessment using the Centers for Medicare Medicaid (CMS) specified Resident Assessment Instrument
(RAI) process within the regulatory timeframe for 1 (R80) of 1 resident reviewed for quarterly resident
assessment in a sample of 29.On 09/11/2025 at 12:56PM, V22 (Minimum Data Set (MDS)/Care Plan
Coordinator) stated the purpose of the MDS is to describe the resident and give a picture of the care a
resident will receive. V22 stated the MDS is submitted to CMS (Centers of Medicare Medicaid) every
quarter (every 92 days) or more frequently if the resident has experienced significant change.V22 stated
R80's ARD (Assessment Reference Date) was completed late and further stated assessment should be
completed within 14 days from the ARD. V22 stated that timing completion of the MDS assessments are
based on the RAI manual.The facility's RAI Version 3.0 Manual dated October 2019 page 2-17 titled RAI
OBRA-required Assessment Summary indicates that Quarterly (Non-Comprehensive) MDS assessment
should be completed no later than 14 days from the ARD.Assessment final validation report dated
7/24/2025 showed Message: Assessment completed late. Assessment completion date is more than 14
days.
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145867
If continuation sheet
Page 3 of 20
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
145867
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/12/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Alta Rehab at Fairmont
5061 North Pulaski Road
Chicago, IL 60630
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0657
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Develop the complete care plan within 7 days of the comprehensive assessment; and prepared, reviewed,
and revised by a team of health professionals.
Based on observation, interview and record review, the facility failed to initiate a person-centered care plan
with appropriate interventions for one resident (R94) of 29.Findings include:9/9/25 at 12:11 PM, Writer
observed R94 lying in bed eating lunch. R94s head of the bed was not upright, it was approximately 30
degrees high. R94 was almost lying flat. R94 was bending at the neck to put food in R94s mouth. Writer
observed R94 coughing as R94 ate and drank. Writer observed signage on the wall above R94s bed that
read in part: remember safe swallowing: sit upright when eating and drinking. R94 said R94 eats like this
every meal. R94 said staff pull R94 up but R94 keeps sliding back down.9/10/25 at 12:22 PM, R94 said
when the head of the bed is up, R94 slides down so there is no point in putting it up. 9/10/25 at 12:28 PM,
V39 (Certified Nursing Assistant) stated R94 always refuses to have the head of bed up while eating. V39
stated V39 has warned R94 of the choking hazard. V39 stated V39 has not told the Director of Nursing or
anyone of R94s preference.9/10/25 at 12:51 PM, V42 (Licensed Practical Nurse) stated V42 is familiar with
R94. V42 stated R94 always wants to lay flat even when eating and for medication administration. V42
stated V42 has educated R94 on the choking, aspiration hazard. V42 stated V42 believes the Director of
Nursing is aware of R94s preference but V42 has not notified the Director of Nursing or
management.9/11/25 at 9:54 AM, V2 (Director of Nursing) stated staff have not made V2 aware that R94
eats lying down. V2 stated R94 is a picky eater as far as food preferences. V2 stated we will make a plan for
R94 to help R94 stay in position, particularly when eating. V2 stated R94s preference should be care
planned. V2 stated whoever is aware of the situation could care plan it. Nurses can care plan it. V2 checked
R94s care plan and stated R94s lying down while eating is not care planned. R94s face sheet provided by
facility indicates R94 has diagnoses that include but not limited to gastro-esophageal reflux disease;
dyspepsia.Facility was not able to provide a care plan that addresses R94s preference to not be positioned
upright while eating.Facility policy Comprehensive Care Plan, 11/17/17, reads in part: To develop a
comprehensive care plan that directs the care team and incorporates the resident's goals, preferences, and
services that are to be furnished to attain or maintain the resident's highest practicable physical, mental,
and psychosocial well-being.
Event ID:
Facility ID:
145867
If continuation sheet
Page 4 of 20
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
145867
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/12/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Alta Rehab at Fairmont
5061 North Pulaski Road
Chicago, IL 60630
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0676
Ensure residents do not lose the ability to perform activities of daily living unless there is a medical reason.
Level of Harm - Minimal harm
or potential for actual harm
Based on observation, interview and record review, the facility failed to properly position one resident (R24)
of 29 reviewed for activities of daily living. Findings include:9/9/25 at 12:23 PM, writer observed R24 lying in
bed with the head of the bed not in an upright position, approximately 30 degrees. R24 was not pulled up in
the bed. R24s lunch tray was on the bedside table across the bed. Writer observed the tray had been eaten
from. Writer observed R24 take spoonsful from the tray and eat them. 9/9/25 at 12:27 PM, V24 (Licensed
Practical Nurse) stated R24s head of bed was almost flat. V24 stated R24 feeds self. V24 stated R24 could
have choked, aspirated with the head of bed low and R24 not positioned upright.9/9/25 at 2:04 PM, V41
(Certified Nursing Assistant) stated residents should not be flat to eat because they could aspirate. V41
stated V41 placed R24s meal tray down and R24 reached for the food to eat. V41 stated next time V41 will
reposition R24 first before giving the meal tray.9/11/25 at 9:54 AM, V2 (Director of Nursing) stated when
setting up a resident to eat, the CNA will set them up. They sit them up in the bed. Elevate the head of the
bed to at least 45 degrees. They put the bedside table in front of the resident with the food tray and drinks
and position everything in their reach. They assess for any other needs before leaving the resident. R24
needs assistance to prop-up in bed. R24 should not be lying in bed to eat.R24s face sheet provided by
facility indicates R24 has diagnoses that include but not limited to dementia; dysphagia, oropharyngeal
phase; fall; presence of artificial hip joint, bilateral.R24s MDS (Minimum Data Set) 8/11/2025, indicates a
BIMS (Brief Interview for Mental Status) score was not able to be obtained due to R24 was unable to
complete the interview. R24 requires setup or clean-up assistance for eating. R24 requires partial/moderate
assistance to go from lying to sitting on the side of the bed.R24 has care plan that reads in part: I have a
swallowing problem related to swallowing assessment results; with intervention including: Instruct resident
to eat in a upright position, to eat slowly, and to chew each bite.Writer requested policies for choking,
aspiration precautions. V1 (Administrator) stated there are no policies of this subject.V2 (Director of
Nursing) stated we do not have a policy for feeding setup in bed.
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145867
If continuation sheet
Page 5 of 20
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
145867
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/12/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Alta Rehab at Fairmont
5061 North Pulaski Road
Chicago, IL 60630
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0677
Provide care and assistance to perform activities of daily living for any resident who is unable.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview and record review, the facility failed to ensure feeding assistance was provided to a
resident on aspiration precaution. This failure affected one (R83) resident reviewed for activities of daily
living (ADL) care out of 29 residents in the final sample.Findings Include: On 9/9/25 at 12:18 PM, R83's in
bed eating lunch independently with head of bed up to 90 degrees. R83's meal ticket reads in part: 1200
fluid restriction with 1:1 [one-to-one] feeding. Surveyor observed a signage posted on R83's closet
documents in part: Feeding-Aspiration precautions. Patient requires 1:1 feeding. Small teaspoon
presentation at a time. Do not provide secondary bites until patient swallows and clears mouth. Do not
leave patient alone with tray.On 9/9/25 at 12:28 PM, R83 was observed still eating lunch unassisted in her
room. Surveyor called the attention of V5 (Certified Nursing Assistance). On 9/9/25 at 2:28 PM, V12
(Speech Pathologist) stated that R83 was discharged from skilled speech therapy services on 7/16/25 and
the recommendation was solid mechanical soft, thin liquids and one-to-one feeding assistance. V12 stated
that R83 needs full staff assistance with feeding and general swallow precaution: upright posture, slow rate,
slow bites and sips. V12 stated R83 is at risk for choking or aspirating if she's not assisted with meals.R83's
clinical records show an admission date of 10/16/24 with included diagnoses but not limited to type 2
diabetes mellitus, Alzheimer's disease, dysphagia oropharyngeal phase, and chronic obstructive pulmonary
disease. R83's order summary report with active orders as of 9/9/25 reads in part: ST [Speech Therapy]
diet clarification: Diet effective 7/8/2025: mechanical soft solids/thin liquids- STRICT ASPIRATION
PRECATIONS- 1:1 FEEDER. R83's ST Discharge summary dated [DATE] documents in part: one to one
feeding with mechanical soft diet. R83's comprehensive care plan documents in part: Eating: My usual
performance is: partial/moderate assist x 1, 1:1 feeder.Surveyor requested for the facility's policies and
procedures for aspiration precaution and ADL care. V1 (Administrator) stated that the facility has no such
policies.
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145867
If continuation sheet
Page 6 of 20
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
145867
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/12/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Alta Rehab at Fairmont
5061 North Pulaski Road
Chicago, IL 60630
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0684
Provide appropriate treatment and care according to orders, resident’s preferences and goals.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview and record review, the facility failed to follow their policy and procedure to (a)
measure upper circumference and exterior catheter length, (b) change midline dressing timely, (c) provide
maintenance flush, and (d) develop comprehensive care plan of midline use for 1 (R12) resident. The
facility also failed to ensure physician's order was followed for a resident (R1) with aspiration precaution.
These failures affected two (R1, R12) residents out of 29 residents in the final sample reviewed for quality
of care.Findings Include:
Residents Affected - Few
R12's admission record showed admit date on 5/9/25 with diagnoses not limited to Malignant neoplasm of
central portion of left male breast, Secondary and unspecified malignant neoplasm of axilla and upper limb
lymph nodes, Secondary malignant neoplasm of retroperitoneum and peritoneum, Secondary malignant
neoplasm of pleura, Malignant neoplasm of abdomen, Malignant pleural effusion, Secondary malignant
neoplasm of unspecified lung, Essential (primary) hypertension, Other ascites, Spontaneous bacterial
peritonitis. MDS (Minimum Data Set) dated 8/13/2025 showed R12's cognition was intact.
On 9/10/25 At 11:02AM Observed R12 resting in bed, alert and oriented x 3, verbally responsive. R12
showed single lumen midline on left upper arm, dressing was dated 8/29/25. He said midline was placed in
the hospital and dressing was never replaced in the facility. R2's midline was never accessed, and no
flushing was done. He said his left arm circumference and midline external catheter was never measured.
On 9/10/25 at 1:32PM V31 (Licensed Practical Nurse / LPN) stated she is working with R12 today. She said
R12 has a midline and dressing was dated 8/29/25.
On 9/11/25 At 9:18AM V2 (Director of Nursing / DON) stated midline dressing should be changed every 7
days to prevent potential infection. She said arm circumference and exterior catheter length of midline
should be measured and documented to monitor complications such as swelling / edema / infiltration or
catheter migration. V2 said midline use should be care planned to establish plan of care and so staff would
know how to care for the resident that would include interventions.
R12's Nurses Note dated 9/8/2025 showed in part: Has IV Midline on the Left forearm.
Care plan reviewed; no plan of care found for R12's midline.
R12's health record reviewed with no documentation found that left arm circumference and external
catheter of midline was measured.
Facility's policy for IV (intravenous) access line maintenance protocol dated 2/7/20 showed in part: Midline:
Maintenance flush for each lumen = 10ml NS (Normal Saline) every week. Transparent dressing changed =
On admission then weekly and as needed. Measure upper arm circumference and exterior catheter length
with each dressing change and prn (as needed).
Facility's comprehensive care plan policy dated 11/17/17 showed in part: to develop a comprehensive care
plan that directs the care team and incorporates the resident's goals, preferences and services that are to
be furnished to attain or maintain the resident's highest practicable well-being.
On 9/9/25 at 10:43 AM, R1 was lying in bed alert and awake noted with bouts of confusion noted.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145867
If continuation sheet
Page 7 of 20
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
145867
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/12/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Alta Rehab at Fairmont
5061 North Pulaski Road
Chicago, IL 60630
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0684
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Surveyor observed a cup of water with a straw on top of R1's bedside table within easy reach of R1.
Surveyor observed a signage posted on top of R1's head of bed.
On 9/9/25 at 10:59 AM, V5 (Certified Nursing Assistant) entered R1's room and stated that the signage
means R1 should not be given a straw with her fluids. V5 stated the cup of water with a straw had been on
top of R1's bedside table since V5 came in the morning. V5 stated, I will take it away from her.
On 9/9/25 at 11:10 AM, V6 (Agency Licensed Practical Nurse) stated that it's her first time working in the
facility. Surveyor showed V6 the signage that was posted on top of R1's bed. V6 stated that the signage
means no straw. V6 confirmed in R1's electronic health records that R1 has an order for NO STRAW
because R1 at risk for aspiration or choking.
On 9/9/25 at 2:28 PM, V12 (Speech Pathologist) stated that R1 was discharged on 8/4/25 from skilled
speech therapy services. V12 stated R1's discharge instruction/recommendation from speech is pureed diet
and thin liquid with no straws. V12 stated staff should be giving R1 a straw because she can aspirate if they
allow R1 to use a straw.
R1's clinical records show an admission date of 3/25/23 with included diagnoses but not limited to
hemiplegia and hemiparesis following other cerebrovascular disease affecting right dominant side,
dysphagia oropharyngeal phase, acute pulmonary edema, and acute bronchitis. R1's Minimum Data Set
(MDS) dated [DATE] shows R1 has impaired cognition and requires supervision assistance for eating.
R1's order summary report with active orders as of 9/9/25 reads in part: GENERAL * diet Pureed * texture,
Thin consistency, NO STRAWS (ordered 7/8/25) and ST (Speech Therapy) diet clarification: puree/nectar to
puree/THIN- NO STRAWS. Administer medications crushed in puree. STRICT NO STRAWS
RESTRICTION- ASPIRATION W/STRAWS. Diet effective: 7/7/2025: Puree solids/Thin liquids- Set up
assist, no straws. R1's comprehensive care plan shows R1 is at risk for aspiration date initiated on 2/21/24.
Surveyor requested for the facility's policy and procedure for aspiration precaution and/or general care. V1
(Administrator) stated that the facility has no such policies.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145867
If continuation sheet
Page 8 of 20
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
145867
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/12/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Alta Rehab at Fairmont
5061 North Pulaski Road
Chicago, IL 60630
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0689
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Ensure that a nursing home area is free from accident hazards and provides adequate supervision to
prevent accidents.
Based on observation, interview and record review, the facility failed to implement fall interventions for two
residents (R24, R151) of 29 reviewed for falls.Findings include:9/9/25 at 12:05 PM, writer observed R151
lying in bed watching television. A fall mat was observed on the floor next to R151's bed. R151's bed was
observed not in the lowest position. R151's bed was approximately knee height. R151 said the bed has
been like this all day. R151 said R151 needs assistance to get out of bed.9/9/25 at 12:23 PM, writer
observed R24 lying in bed and the bed was not at the lowest position. 9/9/25 at 12:27 PM, V24 (Licensed
Practical Nurse) stated R24s bed was raised to about knee level. The bed was not at the lowest position.
V24 stated R24 tries to get up from bed. V24 stated R24 could have fallen out of bed and been injured with
the bed not at lowest position. V24 stated R151's bed should be lower to prevent a fall with injury.9/9/25 at
2:04 PM, V41 (Certified Nursing Assistant) stated R151 is a fall risk because there is a fall mat on the floor
by the bed. The bed should be low for fall precaution because R151 could fall out of bed. 9/11/25 at 9:54
AM, V2 (Director of Nursing) stated R24 is a fall risk. R24's bed should be in the lowest position. V2 stated
R151 is a fall risk. R151's bed should be in the lowest position. The bed should be in the lowest position
because it decreases the risk of significant injury. R151's face sheet provided by facility indicates R151 has
diagnoses that include but not limited to dementia; repeated falls.R151's MDS (Minimum Data Set)
6/23/2025, indicates R151 has a BIMS (Brief Interview for Mental Status) score of 12 indicating moderately
impaired cognition.R151 has care plan that reads in part: Potential for falls related to: confusion, history of
falls, unfamiliar environment, weakness.Fall Risk Assessment, 4/28/2025, categorizes R151 as at risk for
falls.R24's face sheet provided by facility indicates R24 has diagnoses that include but not limited to
dementia; dysphagia, oropharyngeal phase; fall; presence of artificial hip joint, bilateral.R24's MDS
(Minimum Data Set) 8/11/2025, indicates a BIMS (Brief Interview for Mental Status) score was not able to
be obtained due to R24 was unable to complete the interview. R24 requires partial/moderate assistance to
go from sitting to standing.R24 has care plan that reads in part: Potential for falls related to: confusion,
history of falls, unfamiliar environment, weakness.Fall Risk Assessment, 8/11/2025, categorizes R24 as at
risk for falls.Facility policy Fall Prevention Program, 11/21/17, reads in part: To assure the safety of all
residents in the facility, when possible. The program will include measures which determine the individual
needs of each resident by assessing the risk of falls and implementation of appropriate interventions to
provide necessary supervision and assistive devices are utilized as necessary.
Event ID:
Facility ID:
145867
If continuation sheet
Page 9 of 20
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
145867
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/12/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Alta Rehab at Fairmont
5061 North Pulaski Road
Chicago, IL 60630
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0693
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Ensure that feeding tubes are not used unless there is a medical reason and the resident agrees; and
provide appropriate care for a resident with a feeding tube.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, and record review, the facility failed to ensure that the water ordered for flushes is
administered per doctor orders for one (R99) out of five residents reviewed in a total sample of 29. This
failure places residents at risk to be provided with inappropriate care and services to meet the resident's
physical, mental and/or psychosocial needs. Findings include:On 09/09/2025 at 11:21 AM, R99 was
observed laying down on his bed, head of the bed elevated, gastrostomy tube feeding rate set at 65 ml
(milliliter) per hour, water flush set at 160ml every 6 hours. Noted with 599 ml fed and 160 ml flushed. R99's
water flush bag dated 09/08/25 and feeding formula labeled with R99's name, room number, rate, and date
09/08/25. On 09/10/2025 at 11:12 AM, with V25 (Registered Nurse), R99 is not in his room but R99's
g-tube feeding pump noted in R99's room. V25 stated that R99's g-tube is disconnected and turned off
when R99 goes to dialysis. V25 stated I am the one that disconnected it this morning, it was connected
when I came in to work at 7:00 AM. V25 turned on R99's g-tube pump to inform this surveyor the settings
that R99's g-tube pump is set at. V25 stated that R99's g-tube feeding is set at 65ml (milliliter) per hour, and
the water flush is set at 160ml every 6 hours. V25 stated that R99 is being followed by the dietician and V25
does not work regularly with R99. On 09/11/2025 at 10:39 AM, with V2 (Director of Nursing), observed
R99's g-tube feeding pump on and attached to R99. V2 stated I see the water flush is set at 160ml every 6
hours, and the feeding formula is set at 65ml/hour. V2 stated that the feeding and water flush settings
should be cross referenced with the resident's orders. On 09/11/2025 at 9:59 AM, V35 (Registered
Dietician) stated that she is the dietician that follows the residents who are on dialysis. V35 stated that she
recommended for R99 to have a decrease in water flushes because V35 increased R99's gastrostomy
(g-tube) feeding rate. V35 stated that she increased his feeding because R99 was underweight. V35 stated
she decreased water flushes because of heart concerns and total amount of fluid that a dialysis patient can
remove. V35 stated that the feeding tube is already providing fluid. V35 stated that if R99 were to continue
to receive 160ml (milliliters) every six hours of water flushes and 65ml/hour of g-tube feeding, it would be
exceeding the amount of fluids and the blood sodium level will be lower than 135 milliequivalents per liter
(mEq/L).On 09/11/2025 at 9:45 AM, V2 (Director of Nursing) stated that it is important to follow the enteral
orders including flushing orders because it is the residents' nutritional status and it will impact their weights
and overall health. R99's face sheet documents that R99 is a [AGE] year-old individual with diagnoses not
limited to: unspecified protein-calorie malnutrition, gastrostomy status, end stage renal disease,
dependence on renal dialysis, chronic systolic (congestive) heart failure. R99's MDS/Minimum Data Set
Section C dated 07/15/2025 documents that R99 is severely cognitively impaired. R99's active care plan
documents in part R99 requires tube feeding. Interventions document in part I am dependent with tube
feeding and water flushes. See MD (Doctor of Medicine) orders for current feeding orders.R99's nurses
note dated 09/05/2025 12:13 PM documents in part dialysis dietician recommended to decrease water
flush from 160ml every 6 hours to 100 ml every 8 hours. NP (Nurse Practitioner) approved recommendation
noted and carried out. R99's active physician order set documents in part state date 09/05/2025, enteral
feed order every 8 hours 100 ml water flush q 6hrs. Facility document dated 8-3-20 documents in part
gastrostomy tube- feeding and care. To provide nutrients, fluids and medications, as per physician orders, to
residents requiring feeding through an artificial opening into the stomach. Licensed nurse will review
physician's order for type of formula, concentration, rate of flow, and method of administration.
Event ID:
Facility ID:
145867
If continuation sheet
Page 10 of 20
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
145867
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/12/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Alta Rehab at Fairmont
5061 North Pulaski Road
Chicago, IL 60630
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0695
Provide safe and appropriate respiratory care for a resident when needed.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview and record review, the facility failed to ensure a resident (R83) received the correct
oxygen flow rate as ordered by the physician and to ensure nasal cannula tubing was applied to a resident
receiving oxygen for 1 (R1) of 2 residents reviewed for respiratory care in a final sample of 29.Findings
Include:On 9/9/25 at 10:43 AM, R1 was lying in bed alert and awake noted with bouts of confusion. R1's
oxygen (O2) concentrator was turned on and flow rate set to 2 liters per minute (lpm). R1's nasal cannula
(nc) tubing was wrapped around her left side rail; the nasal prong was on the floor and was not applied in
her nose. R1 was not in distress. On 9/9/25 at 10:59 AM, V5 (Certified Nursing Assistant) entered R1's
room and applied the nasal cannula tubing for R1. V5 stated that it should have been in her nose. On 9/9/25
at 10:57 AM, R83's sleeping in bed noted receiving oxygen (O2) via nasal cannula that was set to 3 liters
per minute (lpm).On 9/9/25 at 11:10 AM, V6 (Agency Licensed Practical Nurse) stated that it's her first time
working in the facility. V6 confirmed R83's electronic health record shows an order for continuous oxygen at
2lpm. On 9/10/25 at 11:42 AM, R83 was sleeping in bed and noted her O2 concentrator flow rate was still
set to 3lpm. On 9/10/2025 at 11:52 AM, surveyor asked V14 (Registered Nurse) to check R83's oxygen and
confirmed R83's O2 concentrator flow rate was set to 3lpm. V14 stated the order is 2lpm.9/11/25 at 9:43
AM, V2 (Director of Nursing) stated, When administering oxygen, the nurse is to check the doctor's order.
They must administer and monitor the resident's oxygen based on the doctor's order because it is
considered a medication and if the resident does not need it, it should be removed or if they need it, then it
should be adjusted accordingly. It is important to follow the doctor's order because oxygen falls on
medication safety practice.R1's clinical records show an admission date of 3/25/23 with included diagnoses
but not limited to hemiplegia and hemiparesis following other cerebrovascular disease affecting right
dominant side, acute pulmonary edema, and acute bronchitis. R1's Minimum Data Set (MDS) dated [DATE]
shows R1 has impaired cognition and requires staff assistance with bed mobility and transfers. R1's order
summary report with active orders as of 9/9/25 shows Oxygen 2 lpm/nc every shift (ordered 6/15/25).R83's
clinical records show an admission date of 10/16/24 with included diagnoses but not limited to chronic
obstructive pulmonary disease and chronic respiratory failure with hypoxia. R83's MDS dated [DATE] shows
R83 has moderately impaired cognition and is total dependent on staff's assistance for transfers and bed
mobility. R83's order summary report with active orders as of 9/9/25 reads in part: Oxygen via nasal
cannula on 2LPM (ordered 10/17/24).The facility's Oxygen Concentrator policy (2013) documents in part:
To provide Oxygen for therapeutic use by utilizing a concentrator that converts ambient air to a higher
concentration level of oxygen. Verify and understand the physician's order. Know the flow rate and duration
of use. Adjust the flow meter control knob to the flow setting prescribed by the physician.
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145867
If continuation sheet
Page 11 of 20
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
145867
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/12/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Alta Rehab at Fairmont
5061 North Pulaski Road
Chicago, IL 60630
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0700
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Try different approaches before using a bed rail. If a bed rail is needed, the facility must (1) assess a
resident for safety risk; (2) review these risks and benefits with the resident/representative; (3) get informed
consent; and (4) Correctly install and maintain the bed rail.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview and record review, the facility failed to assess the risk versus benefits of using side
rails and review them with the resident prior to use and failed to implement person-centered comprehensive
care plan addressing the use of the side rails. These failures affected two (R4, R52) out of three residents
reviewed for side rails in a final sample of 29.
Findings Include:
On 9/9/25 at 11:47 AM, R4 was sitting on the side of the bed and noted with two upper half side rails up. R4
stated she gets out of bed by herself and uses a wheelchair to get around.
On 9/10/2025 at 11:37 AM, R4 was sleeping in bed and noted with two half upper side rails up.
On 9/10/25 at 10:43 AM, V22 (MDS Coordinator) stated that the purpose of the care plan is to notify the
staff how to provide care for the residents. V22 stated if the resident has a change in condition the care plan
should be updated as soon as possible. V22 stated that comprehensive care plan should be initiated on
admission MDS (Minimum Data Set), annually, significant change, and with any change in condition. V22
stated that the needs of the resident should be addressed in the care plan and how to provide the care for
the residents. V22 stated the use of side rails should be addressed in the care plan. V22 confirmed in R4's
electronic health records that R4 had no side rails care plan. V22 also confirmed that there was no side rail
assessment completed for R4, and that the last one was done on 6/28/24 from R4's previous admission.
On 9/10/25 at 3:11 PM, V32 (Restorative Nurse) stated that side rail risk assessment should be completed
before using the side rails for the residents. V32 stated that the purpose of the assessment is to determine
for risk of injury when they are using the side rails, to determine if the resident can use the side rails safely
and the benefits of the side rails. V32 stated that a consent obtained from the resident or responsible party
prior using the side rails is incorporated in the side rail risk assessment. V32 stated that side rail risk
assessment is completed upon admission and reviewed on a quarterly basis or if there is a significant
change or as needed. V32 stated that the use of side rails needs to be incorporated in the ADL (Activity of
Daily Living) care plan as part the bed mobility performance. V32 stated that the side rail assessment
needs to be re-evaluated for continued use or for any changes.
R4's clinical records show an admission date of 6/25/25 with included diagnoses but not limited to
dementia, essential hypertension, and chronic kidney disease. R4's Minimum Data Set, dated [DATE]
shows R4 is cognitively impaired and requires substantial maximal assistance from staff for bed mobility
and transferring from bed. R4's physician orders do not have an order for use of side rails. R4's electronic
health records revealed no side rail/s assessment since the admission date of 6/25/25. R4's comprehensive
care plan does not address the use of side rails.
R52's admission record showed initial admit date on 7/26/2024 with diagnoses not limited to End stage
renal disease, Dependence on renal dialysis, Benign prostatic hyperplasia, Essential (primary)
hypertension, Multiple subsegmental thrombotic pulmonary emboli, Unspecified atrial fibrillation,
Obstructive and reflux uropathy, Wedge compression fracture of fourth lumbar vertebra, Wedge
compression
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145867
If continuation sheet
Page 12 of 20
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
145867
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/12/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Alta Rehab at Fairmont
5061 North Pulaski Road
Chicago, IL 60630
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0700
fracture of second lumbar vertebra.
Level of Harm - Minimal harm
or potential for actual harm
MDS (Minimum Data Set) dated 8/6/2025 showed R52's cognition was intact. He needed total assistance
with toileting hygiene, shower / bathe self, lower body dressing; Partial / moderate assistance with upper
body dressing and personal hygiene, roll from lying on back to left and right side, sitting on side of bed to
lying flat on the bed; Dependent with chair / bed transfer.
Residents Affected - Few
On 9/09/2025 at12:36PM Observed R52 in bed, alert and verbally responsive, with 2 upper side rails up.
R52 said rails are always up.
On 9/10/25 At 3:22PM V32 (Restorative nurse) stated side rails should have a care plan. Surveyor reviewed
R52's EHR (Electronic Health Record) with V32 and stated there is side rail assessment indicated for bed
mobility. Stated no care plan found for Side rail use.
On 9/11/25 At 9:18AM V2 (Director of Nursing / DON) said use of bedrails should have an assessment and
usually it is being used to enhance bed mobility. Stated bedrail use should be planned for safety of the
resident and so staff would be able to know the use of bed rails for positioning.
The facility's Side Rails/Bed Rails policy dated 10/24/22 documents in part: The facility shall ensure that
prior to the installation of bed rails, the facility has attempted to use alternatives. After alternatives to bed
rails have been attempted and determined that these alternatives do not meet the resident's needs, the
facility shall assess the resident for the risks of entrapment and possible benefits of bed rails. In addition,
the resident assessment should include an evaluation of the alternatives to the use of a bed rail that were
attempted and how these alternatives failed to meet the resident's assessed needs. The facility shall also
assess the resident's risk from using bed rails. The following includes potential risks regarding the use of
bed rails: Accident hazards, barrier to residents from safely getting out of bed independently, physical
restraint, other potential negative physical outcomes, and other potential negative psychosocial outcomes.
After alternatives have been attempted and prior to installation, the facility shall obtain informed consent
from the resident or if applicable, the resident representative for the use of bed rails. The care plan shall be
developed on an individual basis, and may include but is not limited to the following related to use of bed
rails: Which medical need would be met through the use of bed rails; How often the bed rail is applied,
duration of use, and the circumstances for when it is to be used; How monitoring is provided, and when and
how often the bed rail is to be released and assistance provided for use of the bathroom, walking and range
of motion; What the resident's functional ability is, such as bed mobility and ability to transfer between
positions, to and from bed or chair, and to stand and toilet and staff required for each function that requires
assistance; Identification of interventions to address any potential complications such as physical and/or
psychosocial changes related to the use of the bed rails, such as increased incontinence, decline in ADLs
or ROM, increased confusion, agitation, and depression; Identification of interventions to minimize or
eliminate the use of the bed rails; and Who monitors for the implementation of the use of the bed rails, and
who evaluates and assesses the resident to determine the ongoing need for bed rails, whether the bed rail
use should be gradually decreased, and how the modifications.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145867
If continuation sheet
Page 13 of 20
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
145867
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/12/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Alta Rehab at Fairmont
5061 North Pulaski Road
Chicago, IL 60630
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0759
Ensure medication error rates are not 5 percent or greater.
Level of Harm - Minimal harm
or potential for actual harm
Based on observations, interviews and record reviews, the facility failed to ensure a medication error rate of
less than 5% for three (R55, R58 and R147) of five residents with 12 errors for 35 medication administration
opportunities. This resulted in a medication error rate of 34.29%. The findings include:On 9/9/2025 at
9:44AM Medication administration observation conducted with V6 (Agency Licensed Practical Nurse /
LPN). Observed V6 prepare and administer the following medications to R58: Guaifenesin 400 MG
(milligrams) 1 TabletJanuvia 50 MG 1 TabletClopidogrel 75 MG 1 TableNifedipine 60 MG Extended Release
1 TabletIron ferrous gluconate 27mg 1 TabletEliquis 5 MG 1 Tablet Observed R58 take prepared
medications by mouth.R58's POS (Physician Order Sheet and MAR (Medication Administration Record)
showed medication orders not limited to: Mucinex cough and chest congestion oral capsule 10-200mg give
1 capsule by mouth two times a day at 9AM and 9PM. Ferrous sulfate 325 MG (65 Fe) give 1 tablet by
mouth two times a day at 8AM and 8PM.Observed medication errors due to wrong dose for Mucinex and
Ferrous sulfate. On 9/9/25 at 10:04 AM Observed V6 (Agency LPN) prepared and administered the
following medications to R147: Ferrous fumarate 325 MG 1 Tablet. Senna 1 tablet Aspirin 81 MG chewable
1 Tablet Losartan potassium 100 MG 1 Tablet. Nifedipine 90 MG Extended Release 1 Tablet. Insulin lispro
200 UNT/ML Pen Injector 5 UnitsObserved V6 injected insulin to R147's right side of the abdomen and
R147 took prepared medications by mouth. R147 POS and MAR showed medication orders not limited to:
Senna plus twice a day give 1 tablet by mouth two times a day at 8AM and 8PM. Nifedipine 90 MG
Extended Release give 1 tablet by mouth two times a day at 9AM and 9PM. HUMALOG Kwik pen inject 5
units subcutaneously with meals at 8AM, 12PM and 5PM.Observed medication errors due to wrong time
for the following medications: Senna, Nifedipine, Insulin Humalog.On 9/9/25 At 10:31am Medication
administration observation conducted with V28 (LPN). Observed V28 prepared and administered the
following medications to R55: Sertraline 50mg 1 tabletLinzess 72mcg 1 tabletPolyethylene glycol 1 capful
mixed with waterAllopurinol 100mg 1 tabletAspirin EC 81mg 1 tabletDocusate Sodium 100mg 1
tabletMagnesium oxide 400mg 1 tabletProtonix 40mg 1 tabletRena Vite R1x 1mg 1 tabletSenna plus 1
tabletHydralazine 50mg 1 tabletSpironalactone 50mg 1 tabletCarvedilol 25mg 1 tabletNifedipine ER 60MG
1 TabletMetolazone 2.5mg 1 tabletLosartan 100mg 1 tabletObserved R55 took prepared medications by
mouth.R55's POS (Physician Order Sheet and MAR (Medication Administration Record) showed order not
limited: Docusate sodium 100 MG Oral Capsule [Colace] two times a day at 9AM and 5PM. Pantoprazole
40 MG Delayed Release Oral Tablet give 40mg by mouth two times a day at 9AM and 5PM. Senna oral
8.6mg give 1 capsule by mouth two times a day at 9AM and 5PM. Hydralazine hydrochloride 50 MG Oral
Tablet give 1 tablet by mouth three times a day for hypertension at 8AM, 12PM and 8PM Carvedilol 25 MG
Oral Tablet give 1 tablet by mouth two times a day at 9AM and 5PM. Nifedipine 60 MG Extended Release
Oral Tablet give 1 tablet by mouth two times a day at 9AM and 5PM. Furosemide 80 MG Oral Tablet give 1
tablet by mouth two times a day at 9AM and 5PM.Observed medication errors due to wrong time for the
following medications Docusate sodium, Pantoprazole, Senna, Hydralazine, Carvedilol, Nifedipine.
Furosemide 80 MG was omitted or was not given during medication administration. On 9/11/25 At 9:18AM
V2 (Director of Nursing / DON) stated nurses are expected to follow Medication administration policy by
giving medications in a timely manner. She said nurses have 2-hour window one hour before and one after
the ordered time. V2 said nurses should follow 5 R's (Right resident, route, dose, time, medication) in
medication administration. She said if a nurse is not following doctor's order for the right time and dose in
giving medication it could have a negative impact to the resident. V2 said for example Blood pressure
medication was not given at the ordered time, could potentially lead to hypertensive crisis and trip to the
hospital. She said If insulin was not given in a timely fashion, hyperglycemic incident could occur and
potentially
Residents Affected - Few
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145867
If continuation sheet
Page 14 of 20
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
145867
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/12/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Alta Rehab at Fairmont
5061 North Pulaski Road
Chicago, IL 60630
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0759
Level of Harm - Minimal harm
or potential for actual harm
lead to a trip to the hospital. V2 said if medication dosage was not followed, potentially the resident could
not receive therapeutic effect of the medication.Facility's administration procedure for all medications dated
8/2020 showed in part: Medications will be administered in a safe and effective manner. At a minimum,
review the 5 rights at each of the following steps of medication administration. Check the MAR for the order
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145867
If continuation sheet
Page 15 of 20
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
145867
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/12/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Alta Rehab at Fairmont
5061 North Pulaski Road
Chicago, IL 60630
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0761
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Ensure drugs and biologicals used in the facility are labeled in accordance with currently accepted
professional principles; and all drugs and biologicals must be stored in locked compartments, separately
locked, compartments for controlled drugs.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observations, interviews and record reviews, the facility failed to (a) properly date opened multi-dose insulin
for three (R7, R126 and R137) residents, and (b) ensure multi-dose eye drops were properly stored at
appropriate temperature for two (R35 and R67) from 4 of 8 medication carts and 1 of 2 medication rooms
inspected for medication storage and labeling. The findings include: On n [DATE] at 11:26AM Team 4
Medication cart inspected with V25 (Registered Nurse / RN) and observed the following: R137's multi dose
LANTUS insulin was opened with no open date. Pharmacy label showed once opened refrigerate or not
discard after 28 days. R35's unopened multi dose Latanoprost eyedrop was kept inside the medication cart.
Pharmacy label showed: Refrigerate unopened, store opened at room temperature discard after 6 weeks.
R67's unopened multi dose Latanoprost eyedrop was kept inside the medication cart. Pharmacy label
showed: Refrigerate unopened, store opened at room temperature discard after 6 weeks. V25 said once
insulin was opened it should be dated to know when to discard. She said Unopened Latanoprost eyedrop
should be refrigerated as it is indicated in the pharmacy label. On n [DATE] at 11:43AM Team 1 medication
cart inspected with V27 (Licensed Practical Nurse / LPN) and observed the following: R7's multi-dose dose
Lantus insulin pen was open with no date. Pharmacy label showed: Once opened store at room
temperature for 28 days. R126's multi-dose dose Lantus insulin pen was open with no date. Pharmacy label
showed: Once opened store at room temperature for 28 days.V27 said insulin once opened should be
dated and discarded after 28 days.On [DATE] At 9:18AM V2 (Director of Nursing / DON) stated nurses
should follow recommendation from the pharmacy for proper storage of medication. She said if the
medication needed to be refrigerated then it should be kept in the right temperature. V2 said if medication is
not properly stored at right temperature potentially the effect of the medication could be altered, or the
potency of the medication could be affected. V2 said nurses should date insulin once opened because
insulin is only good for certain days. She said if insulin is not properly dated could potentially give expired
medication to the resident. V2 said Lantus insulin once opened is good for 28 days and should be
discarded. R7's POS (Physician Order Sheet) dated [DATE] showed active order not limited to: Lantus
solution pen injector 100unit/ml inject 32 units subcutaneously at bedtime. R35's POS dated [DATE]
showed active order not limited to: Latanoprost ophthalmic solution instill 1 drop in right eye in the evening.
R67's POS dated [DATE] showed active order not limited to: Latanoprost solution instill 1 drop in both eyes
at bedtime. R137's POS (Physician Order Sheet) dated [DATE] showed active order not limited to: Lantus
solution 100unit/ml inject 36 units subcutaneously two times a day. Facility's storage of medications policy
(undated) showed in part: Medications are stored safely, securely and properly, following manufacturer's
recommendations or those of the supplier. Medications requiring refrigeration are kept in a refrigerator at
temperature between 36F - 46F. Certain medications or package types such as multiple dose injectables
vials, ophthalmic, once opened, require an expiration date shorter than the manufacturer's expiration date
to insure medication purity and potency. Facility's reference guide - medications with shortened expiration
dates dated [DATE] showed in part: Lantus vial - once opened store below 30. Product expires 28 days
after the first use or removal from refrigerator whichever comes first. Lantus pen: once opened, do not
refrigerate. Store at room temperature. Product expires 28 days after the first use or removal from
refrigerator whichever comes first. Latanoprost: store unopened bottles under refrigeration (36F - 46F).
Once opened, product may be stored at room temperature for 42 days.
Event ID:
Facility ID:
145867
If continuation sheet
Page 16 of 20
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
145867
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/12/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Alta Rehab at Fairmont
5061 North Pulaski Road
Chicago, IL 60630
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0812
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Many
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Procure food from sources approved or considered satisfactory and store, prepare, distribute and serve
food in accordance with professional standards.
Based on observation, interview and record review, the facility failed to follow food item labeling practices to
ensure there are no outdated food items in the kitchen for resident consumption. This failure has the
potential to effect 141 residents that receive food from the kitchen.Findings include:9/9/25 at 9:23 AM,
conducted initial tour of kitchen with V40 (Dietary Manager)Observed in milk cooler #1:-one carton of
Thickened Lemon Flavored Water, not sealed, with no Opened date-one carton of Thickened Lemon
Flavored Water, not sealed, with Opened date 8/29/25. V40 stated the flavored water is kept one week after
unsealing.Observed in reach-in refrigerator:-three salad bowls labeled with prep date 9/7/25 and use by
date 9/14/25-two salad bowls labeled with prep date 9/6/25 and no use by date-one salad plate with prep
date 9/6/25 and no use by date-three salad plates with prep date 9/7/25 and use by date 9/14/259/10/25 at
1:07 PM, V43 (Cook) stated we have to put the open and use by date on kitchen items for resident safety.
Salads should be used within three days. Other items seven days. After three days salad can get slimy,
brown and no good. Residents should never get expired foods because of possible food poisoning,
sickness.9/10/25 at 1:14 PM, V40 (Dietary Manager) stated V40 prefers the salads to be made daily and
kept no longer than three days. It is important to label correctly so old food is not given to the residents and
to describe the food. Dating the items tell when the item is to be trashed. If residents are given old food,
there is potential for the resident to get food born illness. The facility has one resident that takes honey thick
water.Facility policy Storage Periods, Use-By Guidelines, no date, reads in part: Food should be stored
properly and used within the appropriate time period to ensure safe and high-quality food is served. The
Use-By Guidelines-Posted should be used to determine a use-by date when labeling opened or unopened
food that must be used within a certain time frame (i.e. not manufacturer use by dates). Foods with a
manufacturer's use-by date should still require an opened-on date once the item is opened. Expired food
items should be disposed of.
Event ID:
Facility ID:
145867
If continuation sheet
Page 17 of 20
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
145867
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/12/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Alta Rehab at Fairmont
5061 North Pulaski Road
Chicago, IL 60630
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0880
Provide and implement an infection prevention and control program.
Level of Harm - Minimal harm
or potential for actual harm
Based on observation, interview, and record review, the facility failed to a) perform hand hygiene before and
after having direct contact with residents and ensure necessary equipment are maintained to carry out an
effective infection control program for five (R14, R55, R58, R140 and R147) of five residents reviewed for
infection control b) ensure that its staff follow proper personal protective equipment (PPE) protocols for one
(R99) out of five residents reviewed in a sample of 29. The findings include:
Residents Affected - Some
On 9/9/25 at 9:44 AM During medication administration observed V6 (Agency LPN / Licensed Practical
Nurse) checked R58's BP (Blood Pressure) = 120/59, PR (Pulse Rate) =77/minute and administered
medications to R58. V6 did not perform hand hygiene before entering / exiting R58's room, and after direct
contact with R58. Standing BP device was not cleaned /disinfected / sanitized after R58's use.
On 9/9/25 at 9:54 AM Observed V6 donned gloves and checked R140's BP = 133/46; PR =71/minute using
the same Standing BP device used with R58. V6 did not perform hand hygiene before entering, exiting
R140's room, donning and doffing of gloves, and after direct contact with R140. Standing BP device was
not cleaned /disinfected / sanitized after R140's use.
On 9/9/25 at 10:05 AM Observed V6 donned gloves and checked R147's BP =104/67; PR = 83 using the
same standing BP device that was not sanitized or disinfected after R58 and R140's used. Observed V6
checked R147's Blood Sugar = 212. V6 removed gloves and did not perform hand hygiene and wore gloves
again. V6 did not perform hand hygiene before entering / exiting R147's room, donning and doffing of
gloves, and after direct contact with R147. Standing BP device was not cleaned /disinfected / sanitized after
R147's use.
On 9/9/25 10:20 AM During medication administration, R14's room with door signage indicated EBP
(Enhanced Barrier Precaution). V28 donned PPEs (Personal Protective Equipment) gloves and gown
without performing hand hygiene. V28 entered R14's room and administered medications to R14. V28
removed PPEs without performing hand hygiene. V28 did not perform hand hygiene before entering /
exiting R14's room, donning and doffing PPEs, and after direct contact with R14.
On 9/9/25 At 10:31 AM Observed EBP door signage on R55's room. V28 donned gloves and gown without
performing hand hygiene. V28 checked R55's BP = 183/65, PR = 57/MIN Temperature = 98.1F and Oxygen
saturation = 98% at room air. V28 did not sanitize / disinfect / clean standing BP device used for R55. V28
was not observed perform hand hygiene before and entering R55's room and direct contact with R55.
On 9/11/25 At 9:18 AM V2 (Director of Nursing / DON) stated staff is expected to perform hand hygiene
when entering and exiting resident's rooms and direct contact with resident to prevent nosocomial infection
/ spread of infection. V2 said reusable medical equipment such as BP, and Pulse oximeter and oxygen
saturation should be sanitized, cleaned or disinfected every after use or in between in resident's use to
prevent cross contamination or spread of infection.
Surveyor attempted to request policy for reusable medical equipment such as BP, Thermometer, Pulse
oximeter to facility but was not able to provide. V1 (Interim Administrator) and V2 (Director of Nursing /
DON) said no policy for such.
Facility's Hand hygiene policy dated 7/30/24 showed in part: Examples of when to perform hand
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145867
If continuation sheet
Page 18 of 20
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
145867
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/12/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Alta Rehab at Fairmont
5061 North Pulaski Road
Chicago, IL 60630
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0880
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
hygiene: At room entry. Before exiting room. Before and after having direct contact with a patient's intact
skin (taking a pulse or blood pressure.
Facility's Infection prevention and control program dated 11/28/17 showed in part: All facility personnel are
required to routinely wash hands. The facility shall assure that necessary equipment are maintained to
carry out an effective Infection Control Program.
On 09/09/2025 at 11:21 AM, CDC (Centers for Disease Control and Prevention) enhanced barrier sign
outside of R99's bedroom door and PPE (personal protective equipment) supplies in a bin outside of R99's
room.
On 09/09/2025 at 11:31 AM, V9 (Certified Nursing Assistant) noted applying gloves, removing R99's
blanket, not wearing gown. Despite this surveyor informing V9 that the surveyor will step out since the
surveyor knows that V9 will need to gown up and gather supplies. Observed R99 with a disposable chuck, a
flat sheet, and a brief that was not placed properly on R99. This surveyor stepped outside of R99's room
and did not observe V9 don on proper PPE as V9 closed the bedroom door. V10 (Certified Nursing
Assistant) opened door to throw soiled linen in a bin a few steps away from R99's room only wearing
gloves, both V9 and V10 were not observed wearing a gown. As V10 opened and closed R99's door, V9 is
not wearing a gown while changing R99's linen. V10 stated that she is new and is an orientee. V10 stated I
was just picking up the dirty briefs and dirty linen. I threw the gloves inside dirty cart and now heading back
inside the room. V10 stated I didn't provide care to R99, I just asked V9 if she needed anything else. V10
stated that she will be washing her hands after she finishes helping V9. V9 opened R99's room door and
asked V10 if she can provide V9 with a clean hospital gown for R99. V9 observed not wearing a gown, only
gloves.
On 09/09/2025 at 11:44AM, V9 (CNA) stated that she has completed providing ADL (activities of daily
living) care to R99. V9 said that she provided the following care to R99, I cleaned him, changed his sheets,
washed his face again, hands. V9 stated that she didn't wear a gown because V9 was already in there. V9
stated I didn't wear it; I should have been wearing one. V9 stated that the importance of wearing proper
PPE (personal protective equipment is for infection control.
On 09/09/2025 at 3:01 PM, V2 (Director of Nursing) stated that enhanced barrier is the biggest one or most
often used one in the facility. V2 stated because anyone that has foley catheters, intravenous (IV), urostomy
tubes, gastrostomy tubes, anything that we are worried the residents getting them infected, requires to wear
a gown and glove when engaging with the patient such as touching the patient.
CDC (Centers for Disease Control and Prevention) enhanced barrier precaution sign reads in part
providers and staff must also: wear gloves and a gown for the following high-contact resident care activities.
Dressing, bathing/showering, transferring, changing linens, providing hygiene, changing briefs or assisting
with toileting.
R99's active physician order set documents in part enhanced barrier precautions for chronic wound.
R99's active physician order set documents in part enhanced barrier precautions for dialysis catheter,
Gtube (gastrostomy tube).
Facility document dated 5/7/24 documents in part Enhanced Barrier Precautions (EBP) refer to an infection
control intervention designed to reduce transmission of multidrug-resistant organisms that
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145867
If continuation sheet
Page 19 of 20
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
145867
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/12/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Alta Rehab at Fairmont
5061 North Pulaski Road
Chicago, IL 60630
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0880
Level of Harm - Minimal harm
or potential for actual harm
employs targeted gown and glove use during high contact resident care activities. For residents for whom
EBP are indicated, EBP is employed when performing the following high-contact resident care activities,
especially when care is being bundled: providing hygiene, changing linens, changing briefs or assisting with
toileting.
Residents Affected - Some
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145867
If continuation sheet
Page 20 of 20