F 0693
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
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.
Based on observation, interview and record review, facility failed to follow their protocol for the labeling of
Enteral tube feeding set-ups and all other equipment used in its conjunction, for nutrition, fluids, and
medications for R30 in a sample of 12 residents.
Findings Include:
On 7/26/22 at 10:42 am, upon tour of XX floor, noted R30 with two bags hanging on pole, noted one as
Isosource 1.5 cal Enteral feeding and the other with clear fluid in approximately 200-300 milliliters (ml). Both
infusing through gastric feeding pump, both bags were noted without labeling of date, time, and initials of
person who hung the items. The bag with clear fluid without details of its contents as well. According to the
resident's orders, 37ml's of water to infuse concurrently with the Enteral feeding of Isosource 1.5 cal. Also
observed irrigation set-up for medication administration and post flushing, was without date, and time.
R30's orders state resident of Nothing by mouth status, part of diagnosis is that of Dysphagia; review of
R30's weight appears stable for last several months.
On 7/27/22 at 03:05 pm, V4 (Registered nurse/RN), working for facility less than 6months, said labeling of
the tube feeding set-ups allows staff to know of its time of expiration, to assure no complications to the
resident. V4 stated, Gastric feeding is good for 24 hours, and feeding set-up to be hung every evening. To
keep any longer can cause illness to the resident and stomach upset with nausea and vomiting.
On 7/28/22 at 03:40 pm, V2 (Nurse Supervisor) said dating of the nutritional supplement is to assure its use
has not gone beyond its expiration of use. Also stated, Any fluids infusing into someone is to be monitored
for length of time of its use, because over time can cause bacterial growth and cause a person to become
ill. The expectation of the labeling to the Enteral nutritional feeding, water flush bags, and is for staff to
follow the policy in its accordance.
Facility's Enteral Feeding Policy, with last review of 11/18/21, states in part:
Make sure that you label the enteral formula container with the patient's identifiers; formula name (and
strength, if diluted); date and time of formula preparation; date and time that you hung the formula;
administration route, rate, and duration (if cycled or intermittent); initials of the person who prepared, hung,
and checked the enteral formula against the order: expiration date and time.
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 6
Event ID:
145637
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
145637
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
07/29/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
St Joseph Village of Chicago
4021 West Belmont
Chicago, IL 60641
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 - Potential for
minimal harm
Based on observation, interview and record review the facility failed to prevent the potential for cross
contamination when using blood glucose supplies. This deficient practice has a potential to affect 4 of 4
(R24, R26, R34, R39) residents reviewed for blood glucose monitoring. The facility also failed to clean the
insulin pen stopper prior to applying the needle for 2 of 2 (R34, R39) review during medication
administration in a sample of 12.
Residents Affected - Some
Findings Include:
R24 has diagnosis not limited to Type 2 Diabetes Mellitus, Chronic Kidney Disease, Bipolar Disorder, Major
Depressive, Dementia and Anxiety Disorder.
Care Plan document in part: R24 has Diabetes Mellitus. Fingerstick blood sugars as ordered.
R24 Physician Order dated 12/18/21 document in part: Blood Glucose Test Strip (Glucose Blood) Inject 1
stick subcutaneously three times a day.
R26 has diagnoses not limited to Type 2 Diabetes Mellitus with Foot Ulcer, Hypertensive Heart and Chronic
Kidney Disease with Heart Failure.
Care Plan document in part: R26 has Diabetes Mellitus.
R26 Physician Order dated 07/18/22 document in part: Blood Glucose Test QID (four times a day).
R34 has diagnoses not limited to Type 2 Diabetes Mellitus with Diabetic Peripheral Angiopathy, Unspecified
Dementia and Depression.
Care Plan document in part: R34 has Diabetes Mellitus.
R34 Physician Order dated 10/26/21 document in part: Blood Glucose Test Strip (Glucose Blood) Inject 1
stick subcutaneously before meals and at bedtime. Novolog Flex pen inject 5 units subcutaneously Twice a
day. Order date 04/29/22.
R39 has diagnoses not limited to Type 2 Diabetes Mellitus and Hypertensive Heart and Chronic Kidney
Disease with Heart Failure.
Care Plan document in part: R39 has Diabetes Mellitus. Administer diabetic medication as ordered. o
Conduct blood sugar testing as ordered.
R39 Physician Order dated 12/14/21 document in part: Humalog Solution 100 UNIT/ML (Milliliter) per
sliding scale. (Insulin Lispro) Inject subcutaneously three times a day. Physician Order dated 12/14/21
Blood Glucose Test Strip (Glucose Blood) Inject 1 strip subcutaneously one time a day
On 07/26/22 at 12:50 PM, V4 (Registered Nurse/RN) removed R39 Insulin Kwik Pen from the medication
cart, removed it from the storage bag, took the Insulin Pen out of the storage bag, removed the cap then
applied the needle to the pen without wiping the stopper with an alcohol wipe.
On 07/26/22 at 01:04 PM, V4 (RN) placed 3 lancets, alcohol wipes, glucometer and blood glucose test
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145637
If continuation sheet
Page 2 of 6
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
145637
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
07/29/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
St Joseph Village of Chicago
4021 West Belmont
Chicago, IL 60641
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 - Potential for
minimal harm
strip container on a white Styrofoam tray then entered R26 room, placed the Styrofoam tray on R26 bed
side table, applied gloves, wiped R26 finger with an alcohol wipe, used 1 lancet to prick R26 finger, picked
up the container of blood glucose strips, removed a strip, placed the blood glucose container back on the
white Styrofoam tray, checked the blood glucose with the glucometer, placed the glucometer back on the
Styrofoam then exited R26 room.
Residents Affected - Some
On 07/26/22 at 01:07, PM V4 (RN) returned to the medication cart, placed the Styrofoam tray on top of the
medication cart, cleaned the glucometer, placed the 2 lancets, alcohol wipes and test strip container on a
clean Styrofoam tray then placed the tray in the medication cart drawer.
On 07/26/22 at 01:11 PM, V4 removed R34 Insulin Flex pen from the medication cart, removed the Insulin
Flex pen from the storage bag, removed the cap from Flex pen then applied a needle to the insulin pen
without cleaning the Flex pen stopper with an alcohol wipe.
On 07/26/22 at 12:15 PM, V4 (RN) stated I should clean the insulin pen with alcohol to make sure it is clean
because it just has the cap on it and is not sterile. There are four residents on the XX floor that have
glucose monitoring, R24, R26, R34 and R39. I take the Styrofoam tray with the glucose monitoring supplies
(lancets, alcohol wipes, glucose strips) and glucometer into the resident's room. By taking the glucose
monitoring supplies into multiple resident rooms there is a potential for cross contamination.
On 07/27/22 at 04:25 PM, V1 (Administrator) stated we do not have an insulin Flex pen/Kwik pen Policy. I
will check with corporate about the policy for the insulin pen.
On 07/28/22 at 11:02PM, V2 (Nursing Supervisor Clinical Service) stated before the needle is applied to
the insulin pen the stopper should be rubbed with an alcohol swab for aseptic technique. The stopper could
have accumulated a bacterial film. Cleaning the stopper is to make sure it is clean and do not transmit
bacteria to the patient. Only the blood glucose equipment that is needed should be taken into the resident's
room. No equipment should come back out of the resident's room except for the glucometer. This is to
minimize any bacteria or contamination and we do not want to introduce any germs a resident may have
into the facility. There is a potential for cross contamination.
On 07/28/22 at 02:08 PM, V1 (Administrator) stated the alcohol swab thing for the insulin pen, the nurse
was nervous and made a mistake. An in-service was given to the nurse and staff. There is no insulin pen
policy.
In Service document titled Proper Technique in Giving Insulin Injection (Sanitation) dated 07/26/22 and
07/27/22 was reviewed.
Policy:
Titled Blood Glucose Monitoring, Long - Term Care reviewed 11/18/21 document in part: Single - use, auto
disabling fingerstick devices should also be used to prevent the spread of bloodborne pathogens.
Implementation: Gather and prepare the necessary equipment and supplies. To collect a sample from the
resident's fingertip, position a single - use auto disabling lancet on the resident's fingertip. Contaminated
blood glucose monitoring equipment increases the risk of transmitting infections cause by bloodborne
pathogens, such as hepatitis B, Hepatitis C, and human immunodeficiency viruses.
Titled Medication Administration - Specific Procedures revised 01/15 document in part: Proper
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145637
If continuation sheet
Page 3 of 6
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
145637
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
07/29/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
St Joseph Village of Chicago
4021 West Belmont
Chicago, IL 60641
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
medication administration techniques should be used regardless of who administers the medication.
Subcutaneous Administration: 1) Swab vial stopper with alcohol wipe.
Level of Harm - Potential for
minimal harm
Residents Affected - Some
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145637
If continuation sheet
Page 4 of 6
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
145637
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
07/29/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
St Joseph Village of Chicago
4021 West Belmont
Chicago, IL 60641
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 0883
Develop and implement policies and procedures for flu and pneumonia vaccinations.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview and record review, the facility failed to follow their immunization policy by not providing pneumonia
vaccines to three (R141, R2, R38) out six residents reviewed for immunizations in a sample of 12 residents.
Also, the facility failed to provide the influenza vaccine to one (R21) out six residents reviewed for
immunizations in a sample of 12 residents.
Residents Affected - Some
Findings Include:
On 07/27/2022 at 10:44 AM, immunization information for the pneumonia and influenza vaccines were
requested for R141, R2, R38, and R21 from V1 (Executive Director) and V2 (Nursing Supervisor Clinical
Services).
On 07/29/2022 at 12:41 PM, V1 stated he was unable to locate the pneumonia information for R141, R2,
R38.
On 07/29/2022 at 02:29 PM, V1 provided an influenza consent for R21 dated 07/29/2022. R21's influenza
consent for the 2021-2022 flu season was not provided by the facility.
On 07/29/2022 at 12:41 PM, V1 (Executive Director) stated, all residents are offered the pneumonia
vaccine upon admission. There should be documentation of refusal and education. All residents are offered
the influenza vaccine during flu season and there should be documentation and education.
Review of the entire electronic medical records (EMR) of the four (R141, R2, R38, R21) residents residing
in the facility during the survey revealed there was no information that addressed the current pneumonia
vaccination status for R141, R2, and R38, and there was no information that addressed the 2021-2022
influenza vaccine status for R21. The review included, but was not limited to, physician orders,
resident/resident representative consents for influenza and pneumonia immunization, immunization tab and
medication administration record (MAR).
R141 was admitted to the facility on [DATE], with diagnoses not limited to, Other Intraarticular Fracture of
Lower End of Right Radius, Subsequent Encounter for Closed Fracture with Routine Healing. Review of
R141's medical record showed no pneumonia consent or refusal documentation.
R2 was admitted to the facility on [DATE], with a diagnosis not limited to, Benign Prostatic Hyperplasia
without Lower Urinary Tract Symptoms. Review of R2's medical record showed no pneumonia consent or
refusal documentation.
R21 was admitted to the facility on [DATE], with a diagnosis not limited to, Atherosclerotic Heart Disease of
Native Coronary Artery without Angina Pectoris. Review of R21's medical record showed no Influenza
consent or refusal documentation for the 2021-2022 flu season.
R38 was admitted to the facility on [DATE], with a diagnosis not limited to, Atherosclerotic Heart Disease of
Native Coronary Artery without Angina Pectoris. Review of R38's medical record showed no pneumonia
consent or refusal documentation.
Facility policy titled, Immunization Program, reads:
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145637
If continuation sheet
Page 5 of 6
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
145637
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
07/29/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
St Joseph Village of Chicago
4021 West Belmont
Chicago, IL 60641
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 0883
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
Franciscan Ministries offers, as available, immunizations against seasonal influenza, other novel/pandemic
influenza and pneumococcal pneumonia to all residents and associates.
The time frame for immunizations against seasonal influenza is generally considered to be from October
1st of each year through March 31st of the following year. In certain circumstances, and with certain
viruses, the season may be extended to an earlier or later date.
A pneumococcal immunization will be offered to residents upon admission unless medically
contraindicated. The type and sequencing of pneumococcal immunizations will depend on the resident's
age, the type of prior pneumococcal immunization and in accordance with current Centers for Disease
Control (CDC) guidelines and recommendations.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
145637
If continuation sheet
Page 6 of 6