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 record review, the facility failed to ensure dignity was maintained by
administering an injection in the dining room for one of six residents (R35) reviewed for medication
administration on the sample list of 25.
Findings Include:
On 6/22/22 at 8:34 AM, V7 RN (Registered Nurse) prepared R35's ordered insulin injections and entered
the dining room to administer it. R35 was sitting at the dining room table with R44 when V7 stated V7
needed to administer R35's insulin. R35 lifted R35's shirt to make R35's abdomen accessible to V7, and V7
administered the two insulin injections.
On 6/22/22 at 8:44 am, R35 stated, staff normally don't give R35 insulin in the dining room but instead
make R35 go to R35's room to get it.
On 6/22/22 at 1:38 pm, V1 Administrator stated the facility does not have a policy for dignity.
On 6/23/22 at 8:30 am, V10 RN (Registered Nurse)/Director of Senior Services stated we {facility} prefer
staff not give injections in the dining room but there are some residents who request it though due to not
wanting to go back to their room. V10 stated those wishes should be care planned.
R35's Care Plan dated 5/18/21 does not document that R35 wishes to have R35's insulin administered in
the dining room.
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 10
Event ID:
145794
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
145794
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
06/23/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Fairview Haven
605 North 4th Street
Fairbury, IL 61739
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 0656
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Develop and implement a complete care plan that meets all the resident's needs, with timetables and
actions that can be measured.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview and record review the facility failed to develop a comprehensive care plan for anticoagulant
therapy for one of 13 residents (R19) reviewed for care plans in the sample list of 25.
Findings include:
The facility's Care Plan - Comprehensive policy dated 3/28/19 documents, Policy Statement(:) An
individualized comprehensive care plan that includes measurable objectives and timetables to meet the
resident's medical, nursing, mental and psychological needs is developed for each resident. 2. The
comprehensive care plan is based on a thorough assessment that includes, but is not limited to, the MDS
(Minimum Data Set). 3. Each resident's comprehensive care plan is designed to: a. Incorporate identified
problem areas; b. Incorporate risk factors associated with identified problems; 5. Care plan interventions are
designed after careful consideration of the relationship between the resident's problem areas and their
causes. When possible, interventions address the underlying source(s) of the problem area(s), rather than
addressing only symptoms or triggers. It is recognized that care planning individual symptoms or Care Area
Triggers in isolation may have little, if any, benefit for the resident. 7. The resident's comprehensive care
plan is developed within seven (7) days of the completion so the resident's comprehensive assessment
(MDS). 8. Assessments of residents are ongoing and care plans are revised as information about the
resident and resident's condition change.
R19's Order Summary dated 6/21/22 documents diagnoses including Chronic Embolism and Thrombosis of
Unspecified Vein, History of Falling and Dementia without Behavior Disturbances. R19's Order Summary
documents orders to obtain PT/INR (Prothrombin Time/International Normalized Ratio) on 7/7/22, one time
only. This Order Summary documents orders for Coumadin (anticoagulant) 2 mg (milligrams) by mouth,
every evening on Monday, Tuesday, Wednesday, Thursday and Friday. This Order Summary also
documents an order for Coumadin 3 mg by mouth every evening on Saturday and Sunday.
R19's Minimum Data Set (MDS) dated [DATE] documents resident is moderately cognitively impaired and
this MDS documents that R19 receives an anticoagulant seven days a week.
R19's Care Plan provided on 6/22/22 by V3 Director of Nursing does not document anticoagulant therapy
for the treatment of Chronic Embolism and Thrombosis or the risk of bleeding and any interventions to
prevent bleeding.
On 6/23/22 at 9:05 AM, V9 Clinical Care Coordinator/Care Plan Coordinator confirmed that R19's
anticoagulant therapy is not on R19's Care Plan. V9 stated that it should be on there because R19 has a
history of having an Embolism.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145794
If continuation sheet
Page 2 of 10
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
145794
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
06/23/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Fairview Haven
605 North 4th Street
Fairbury, IL 61739
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
record review, observation, and interview, the facility failed to keep a resident's oxygen tubing off the floor
and failed to label portable oxygen tubing according to facility policy. This failure affects two of three
residents (R14 and R16) reviewed for respiratory care on the sample list of 25.
Residents Affected - Few
Findings include:
1.) On 06/21/22 at 11:22 AM R14 was seated in a wheelchair at the side foot area of R14's bed. R14 had
an oxygen bedside concentrator that was plugged into the wall outlet at the head of the bed. R14 had a
portable oxygen tank on the back of R14's wheelchair. The bedside oxygen concentrator tubing was stretch
out on the floor three feet from the concentrator to reach R14's wheelchair. The oxygen concentrator tubing
had several feet of oxygen tubing coiled on the floor at the side of R14s wheelchair. R14 stated R14 just
changed over to the portable oxygen in preparation to leave R14's room. R14 stated The oxygen tubing
dangles from the concentrator and onto the floor sometimes. R14's portable oxygen with the nasal cannula
tubing was not dated to indicate when it was last changed. R14 stated R14 is not sure when the portable
concentrator tubing was last changed.
R14's Minimum Data Set (MDS) dated [DATE] documents the following: Brief Interview of Mental Status
score of 13 out of 15, indicating no cognitive impairment
R14's Diagnoses Sheet dated 4/8/22 documents the following: Pulmonary Fibrosis Unspecified.
R14's Physician Order Summary Report Sheet dated as active 6/13/22 documents the following: Resident
(R14) uses O2 (oxygen) per NC ( nasal cannula) at 2L (two liter per minute) when at rest. Increase oxygen)
to 3L (three liter per minute) with activity.
2.) R16's Physician Order Summary Report Sheet (POS) dated June 1/30/22 documents the following
diagnoses and oxygen order: Acute Respiratory Failure Unspecified Whether Hypoxia or Hypercapnia,
Down Syndrome Unspecified, Muscle Weakness Generalized, and Chronic Obstructive Pulmonary
Disease. The same POS documents: May use O2 (oxygen)per NC (nasal cannula) at 2.5L (2.5 liters per
minute) when at rest and up to 4L (four liters)
with walking to keep SpO2 (oxygen saturation) greater than 90%. Active 12/14/2021.
On 06/21/22 12:15 pm - 12:40 pm R16 was feeding herself in dining room. R16's portable oxygen tank was
attached to the back of R16's wheelchair and was in the on position, administering 2.5 liters per minute via
nasal cannula. The oxygen tubing that attached the nasal cannula to the portable oxygen tank had several
feet of excess oxygen tubing that dropped to the floor. The oxygen tubing on floor was directly behind R16's
wheelchair tire and was partially coiled.
On 6/21/22 at 12:40 pm R16 's oxygen tubing continued to lay on the floor. Several unidentified staff
members passed by R16. V5, Registered Nurse acknowledged R16's oxygen tubing was on the floor. V5,
Registered Nurse stated All oxygen tubing and humidifier bottle are dated when they are changed weekly.
The oxygen tubing is never supposed to be on the floor. It can be a trip hazard as well as an infection
control issue.
On 6/23/22 at 3:15 pm V2, Director of Nursing (DON) stated residents' oxygen tubing should never be
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145794
If continuation sheet
Page 3 of 10
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
145794
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
06/23/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Fairview Haven
605 North 4th Street
Fairbury, IL 61739
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
on the floor.
Level of Harm - Minimal harm
or potential for actual harm
The facility policy Oxygen Procedures dated January 12, 2018, documents the following:
5. Date the humidifier bottle and tubing.
Residents Affected - Few
6. Ensure there is a storage bag attached to the concentrator for storage of unused nasal cannula and
excess tubing.
7. Change tubing and nasal cannula /mask every two weeks ,or as needed.
8. Change the humidifier bottle every two weeks, or as needed.
9. Place nasal cannula/mask and excess tubing in the storage bag attached to the concentrator when not in
use. Tubing should not rest on the floor.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145794
If continuation sheet
Page 4 of 10
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
145794
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
06/23/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Fairview Haven
605 North 4th Street
Fairbury, IL 61739
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 0758
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
Implement gradual dose reductions(GDR) and non-pharmacological interventions, unless contraindicated,
prior to initiating or instead of continuing psychotropic medication; and PRN orders for psychotropic
medications are only used when the medication is necessary and PRN use is limited.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview and record review, the facility failed to ensure PRN (as needed) medications were not ordered for
more than 14 days maximum duration permitted for PRN medications without justification, failed to
complete a psychotropic medication assessment prior to starting a psychotropic medication, and failed to
care plan non-pharmacological interventions to assist with behavior management for three of five residents
(R27, R30, and R36) reviewed for psychotropic medications on the sample list of 25.
Findings include:
1.) R36's Physician Order Summary Report Sheet (POS) dated June 1-30, 2022, documents the following
diagnosis: Unspecified Dementia Without Behavioral Disturbance, Anxiety Disorder Due to Known
Physiological Condition, and Delusional Disorder.
R36's Physician Order Summary Report Sheet (POS) dated February 1-28, 2022, documents the following
psychotropic medication order: Lorazepam Tablet 0.5 MG( milligram) Give 1(one) tablet by mouth as
needed (PRN) for Anxiety take every 12 hours. Active 2/01/22. There is no physician order to discontinue or
change the as needed (PRN) Lorazepam medication order after the maximum required duration for prn
psychotropic medications.
R36's Note To Attending Physician/Prescribe documented by V12, Pharmacist, signed by V11, Physician on
03/24/22, documents the following: Resident was started on Lorazepam 0.5 milligrams q (every) 12 hours
added 2/8/22 (actual order as noted on February 2022 POS above has a start date of 2/1/22). The same
Note To Attending Physician/Prescribe documents: Please provide a rational and duration for a PRN
psychotropic order that exceeds 14 days per CMS requirements as indicated above.
V11, Physician documented duration updated as 180 days for intermittent anxiety (dated 3/24/22). As
documented below, R36 received 31 doses after the 14 day maximum duration.
R36's Medication Administration Record dated February 1-28, 2022, documents R36 received prn
Lorazepam 0.5 mg, 31 times after the 14 day maximum prn order permits. R36 Lorazepam administration
occurred on the following dates: February 15-19, 21-24, and the 27, 2022.
R36's Medication Administration Record dated March 1-31, 2022, documents R36 Lorazepam was also
administration on the following dates, March 1-13th, March 15-23, 2022.
On 6/23/22 at 9:45 am V10, Director of Clinical Services/ Registered Nurse and V2, Director of Nursing
(DON) confirmed R36 was admitted to the facility on [DATE] with an order for Lorazepam 0.5 mg by mouth,
as needed every 12 hours. V2 and V10 acknowledged R36's Lorazepam order did not document the 14 day
maximum duration. V2, DON and V10, Director of Clinical Services/RN also confirmed R36 continued to
receive administration of Lorazepam 0.5 mg po every 12 hours until V11, Physician responded to V12,
Pharmacist request to provide a rational and duration for a psychotropic order that exceeds 14 days as
required by CMS.2. R30's Physician Order Recap dated June 2022 documents the following orders:
5/13/22 Cymbalta {Antidepressant} 30 mg (milligrams) daily for depression
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145794
If continuation sheet
Page 5 of 10
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
145794
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
06/23/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Fairview Haven
605 North 4th Street
Fairbury, IL 61739
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 0758
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
6/3/22-6/16/22 Lorazepam Concentrate {Benzodiazepine} 2 mg/ml (milliliters) - give 0.25 ml every 4 hours
PRN for agitation
5/13/22 Trazodone {Serotonin Modulator} 50 mg - give 0.5 tablets every HS (bedtime) for sleep
R30's medical record does not contain a psychotropic medication assessment prior to starting the above
medications.
R30's Care Plan dated 5/11/22 documents R30 requires mood/behavior monitoring due to yelling out and
situations of anger. This Care Plan documents interventions of implementing the above medications but
does not include any non-pharmacological interventions.
On 6/22/22 at 3:13 PM, V7 RN (Registered Nurse)/Psychiatric Nurse explained that when R30 returned
from the hospital on 4/28/22, R30 was not on any psychotropic medications but then hospice
recommended R30 be started on the above medications. V7 stated there should have been a justification
assessment completed at that time but V7 doesn't see that one was completed, (after checking the
computer). V7 also confirmed R30's psychotropic care plan does not include any non-pharmacological
interventions.
3. R27's Order Summary Report dated June 22, 2022, documents an order for Lorazepam {
Benzodiazepine} 0.5 mg - one tablet every three hours PRN for anxiety and shortness of breath until
7/14/22 due to resident being on Hospice.
R27's Progress Notes dated 4/25/22 by V5 RN (Registered Nurse) documents R27 has been discharged
from hospice due to no longer being terminally ill, and R27's condition is stable.
On 6/22/22 at 3:13 PM, V7 RN/Psychiatric Nurse stated when a resident comes off of hospice, they should
be re-evaluated for the use of the PRN psychotropic medication, to ensure they still need them and to
adjust the length of time medications are ordered for.
R27's medical record does not contain a psychotropic medication assessment since being discharged from
hospice services.
The facility Psychotropic Medication Use Policy dated May 13, 2022, documents the following: Physicians
and mid-level providers will use psychotropic medications appropriately, working with the interdisciplinary
team to ensure appropriate use, evaluation and monitoring. Psychotropic medication refers to drugs which
are used for anti-psychotic, anti-depressant, anti-anxiety, and/or hypnotic purposes. It is the policy of this
facility to keep each resident's medication regime free from unnecessary drugs, yet we support the
appropriate use of psychopharmacologic medications that are therapeutic and enabling for residents
suffering from mental illness. Psychotropic medications will not be administered for the purpose of
discipline, staff convenience and will only be used when it is necessary to treat a specific condition. The
facility supports the goal of determining the underlying cause of behavioral symptoms so the appropriate
treatment of environmental, medical, and/or behavioral interventions, as well as psychopharmacological
medications can be utilized to meet the needs of the individual resident. The resident's need for the
psychotropic medication will be monitored by the Psychotropic Drug Monitoring Team. The monitoring will
include: * Identification and daily monitoring of the resident's behaviors that the psychotropic drug could
conceivably address (i.e., target behaviors). * Assessment of potential causes of the behaviors that , if
addressed, could eliminate the behaviors without the use of psychotropic drugs.* Discussion of
non-medical behavior management strategies
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145794
If continuation sheet
Page 6 of 10
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
145794
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
06/23/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Fairview Haven
605 North 4th Street
Fairbury, IL 61739
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 0758
Level of Harm - Minimal harm
or potential for actual harm
that could be implemented in an attempt to reduce/eliminate the behaviors prior to the initiation of drug
treatment as well as on an ongoing basis. This policy also documents, Policy Interpretation and
Implementations number 8. Orders for PRN (as needed) psychotropic medications will be time limited (i.e.,
times two weeks) and only for specific clearly documented circumstances.
Residents Affected - Some
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145794
If continuation sheet
Page 7 of 10
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
145794
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
06/23/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Fairview Haven
605 North 4th Street
Fairbury, IL 61739
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 observation, interview and record review, the facility failed to administer medications according to
Manufacturers Recommendations and facility policy for one (R35) of six residents reviewed for medication
administration in the sample list of 25. The facility had 2 errors out of 33 opportunities for a medication error
rate of 6.06%.
Residents Affected - Few
Findings Include:
R35's June 2022 POS (Physician Order Sheet) documents orders for Lantus {Long Acting Insulin} 10 units
SQ (Subcutaneously) every morning and Novolog {Rapid Acting Insulin} 100 units /ml per sliding scale
coverage SQ before meals and at bedtime{based on blood glucose level}: 151-175 = 1 unit, 176-200 = 2
units, 201-225 = 3 units, 226-250=5 units, 251-275=7 units, 276-300 = 9 units, 301-325 = 12 units,
326-350=15 units, and if greater than 351, call physician
On 6/22/22 at 8:34 AM, V7 RN (Registered Nurse) stated V7 had already checked R35's blood glucose
level, which was 162, therefore R35 would be receiving one unit of Novolog. V7 pulled an unlabeled
Novolog Flexpen from the medication cart and prepared the ordered Novolog. At this time, V7 stated V7
knew it was R35's as it was in the bag with R35's name on it. V7 pulled a bag from the medication cart that
contained needles for the Flexpen and an unlabeled Lantus pen. The bag had a worn pharmacy label on it
which included R35's name, which was barely legible and no other information, due to it being worn. V7
then pulled up 10 units of Lantus from the unlabeled Lantus Pen that was in the bag. At 8:44 am, after the
medication was prepared, V7 administered the medications to R35. R35 had R35's breakfast plate on the
table in front of R35, which was empty. R35 stated R35 had already finished breakfast as it was served
around 7:45 am {an hour prior}. R35 stated this is not unusual, they always give me (R35) insulin after
eating.
The Manufacturers Recommendations for NovoLog dated March 2008 documents Novolog should be given
immediately (within 5-10 minutes) prior to the start of a meal.
The facility's undated Administering Medications Policy documents medications must be administered in
accordance with the orders, including any required time frame. This policy also documents the individual
administering the medications must verify the right medication, right dosage, right time and right method
before giving the medications.
The facility Labeling of Medication Containers Policy dated June 2020 documents medication labels must
be legible at all times. Labels shall include all necessary information such as: the resident name,
prescribers name, pharmacy information including name/address/telephone number, the
name/strength/quantity of the medication, prescription number, and expiration date.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145794
If continuation sheet
Page 8 of 10
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
145794
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
06/23/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Fairview Haven
605 North 4th Street
Fairbury, IL 61739
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 - Few
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.
Based on observation, interview and record review, the facility failed to ensure medications are labeled
appropriately for one of six residents (R35) reviewed for medication labeling in the sample list of 25.
Findings Include:
The facility Labeling of Medication Containers Policy dated June 2020 documents medication labels must
be legible at all times. Labels shall include all necessary information such as: the resident name,
prescribers name, pharmacy information including name/address/telephone number, the
name/strength/quantity of the medication, prescription number, and expiration date.
On 6/22/22 at 8:34 AM, V7 RN (Registered Nurse) prepared R35's morning medications which included
insulin's: Novolog {Rapid Acting Insulin} and Lantus {Fast Acting Insulin}. V7 pulled the unlabeled Novolog
and Lantus from a bag in the medication cart that had a worn pharmacy label on it. The label had R35's
name on it, which was barely legible due to being worn and no other information. V7 stated, V7 knew that
the Novolog and Lantus belonged to R35 due to being in the bag that was labeled for R35.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145794
If continuation sheet
Page 9 of 10
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
145794
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
06/23/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Fairview Haven
605 North 4th Street
Fairbury, IL 61739
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
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 maintain equipment and utensils in
a safe, clean, sanitary condition to prevent the potential for cross-contamination of food from physical
contaminants. These failures have the potential to affect all 47 residents in the facility.
Findings include:
1.) On 6/21/2022 at 9:45 am on tour of the kitchen, accompanied by V8, Dietary Manager, there was a
manual tabletop can opener. The tabletop can opener had thick, dark brown grease-like build-up on the
blade and an accumulation of metal shavings in gears. V8, Dietary Manager stated I see the metal
shavings. I will get that taken care of right away. That is bad and is a potential hazard that could affect all
the residents in the facility.
2.) On 6/21/2022 at 9:50 am continuing on the tour of the kitchen accompanied by V8, there was one large
24 inch by 18 inch acrylic cutting board and two smaller 18 inch by 12 inch acrylic cutting boards. The three
cutting boards each had deep slice-like divots over the majority of the boards The center sliced divot had
imbedded builds-up of brown and yellow food-like debris in the slice-like crevices. V8, Dietary Manager
stated These (cutting boards) need to be thrown out. I will replace them. They can't be used in that
condition.
3.) On 6/21/22 at 9:55 am continuing on the tour of the kitchen accompanied by V8, there were four large
rubber spatulas. The four large rubber spatulas had slice-like divots with food-like debris. The same four
rubber spatulas had uneven chew-like pieces of the rubber missing at the edges. V8, Dietary Manager
stated I have to throw those (spatulas) away too. They can't be used.
The facility policy Cleaning Instruction: Can Opener dated 2020 documents the following:
2. Protocol for counter-mounted can openers:
* Remove can opener shaft from the base; wash in sink with soap and water.
* Pay close attention to the blade and other moving parts.
* Rinse, sanitize and air dry.
* Wash the base carefully with mild detergent and hot water; be sure to get rid of all food particles from the
blade and the base.
* Sanitize and then air dry.
* Reassemble can opener once dry.
The Resident Census and Conditions of Residents report dated 6/21/22 documents 47 residents reside in
the facility.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145794
If continuation sheet
Page 10 of 10