F 0580
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Immediately tell the resident, the resident's doctor, and a family member of situations (injury/decline/room,
etc.) that affect the resident.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, and record review the facility failed to ensure residents' representatives were notified
of a change in resident's condition in 1 of 2 residents reviewed for changes in condition, Resident #56
Findings:
Review of the medical record indicated Resident #56 was admitted to the facility on [DATE] and had a
hospitalization from 12/31/2021 through 1/7/2022. Diagnosis included anemia, hypertension, atrial
fibrillation (an irregular heartbeat), heart failure (a chronic condition where the heart doesn't pump blood as
well as it should), major depression, and dysphagia (difficulty swallowing foods or liquids).
Review of Resident #56's vital signs document weights of 150.2 pounds on 1/12/2022, 141.4 pounds on
2/7/2022, 138 pounds on 3/22/2022, 135 pounds on 3/29/2022 a weight of 132 pounds on 4/8/2022 and a
weigh of 131 pounds on 4/12/2022.
Review of the nursing progress note dated 3/18/2022 read: [ Advanced Practice Registered Nurse's
(APRN) name] saw [Resident #56's name] today and gave recommendations to increase Remeron to 7.5
mg by mouth twice a day secondary to poor appetite. This recommendation was approved by [APRN's
name]. She had previously given orders for an increase in Ready care, lab work and ST (speech therapy)
eval. [evaluation]
Review of Resident #56's medical record did not provide for documentation the resident's
representative/guardian was notified of the resident's weight loss of 19.8 pounds over a period of three
months.
On 4/20/2022 at 11:30 AM Staff H, Registered Nurse (RN) stated, I do not see any notification to her
guardian in the medical record related to her weight loss.
On 4/21/2022 at 12:45 AM the Director of Nursing stated, All changes in condition should have notification
to the physician and the resident or resident's representative.
Review of the policy and procedure titled, Change in a Resident's Condition or Status approval date
2/17/2022 read, Policy: The Center shall promptly notify the resident, his or her attending physician, and
representative of changes in the resident's condition/status. Policy interpretation and implementation: 2.
Unless otherwise instructed by the resident, the nurse supervisor will notify the resident's representative
when: b. There is a significant change in the resident's physical, mental or
(continued on next page)
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 8
Event ID:
105613
Printed: 05/28/2026
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
105613
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
04/21/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Live Oak Healthcare and Rehabilitation Center
1620 Helvenston St SE
Live Oak, FL 32064
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 0580
psychological status.
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105613
If continuation sheet
Page 2 of 8
Printed: 05/28/2026
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
105613
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
04/21/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Live Oak Healthcare and Rehabilitation Center
1620 Helvenston St SE
Live Oak, FL 32064
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 0690
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
Provide appropriate care for residents who are continent or incontinent of bowel/bladder, appropriate
catheter care, and appropriate care to prevent urinary tract infections.
Based on observation, interview, and record review, the facility failed to ensure care and services were
provided for an indwelling urinary catheter for 1 of 3 residents sampled for urinary indwelling catheter care,
Resident #53.
Findings:
Observation on 4/18/2022 at 11:27 AM revealed Resident #53 is in bed, awake, alert, oriented to name,
time, and place. The resident has an indwelling urinary catheter connected to a bedside drainage bag
draining amber colored, cloudy urine.
Interview with Resident #53 on 4/19/2022 at 12:49 PM the resident stated, They do not clean my catheter
every shift. The aide cleaned my catheter when she gave me a bath this morning. I do not refuse catheter
care, not at all. I do not want them to touch my things in my room. I also refuse to get out of bed, but I do
not refuse the cleaning of my catheter. They only provide catheter care when they give me a bed bath, this
is not every day, only if I get a bed bath.
Review of the physician's order dated 11/18/2019 reads: Foley catheter care every shift. Foley catheter size
16 French to bedside drainage. Check for patency every shift and change prn [as needed]. Change Foley
catheter PRN for leakage and blockage as needed for neurogenic bladder.
Observation with Staff B, Certified Nursing Assistant (CNA) and Staff F, CNA on 4/20/2022 at 9:30 AM of
catheter care for Resident #53 showed when Staff B exposed the perineal area, Resident #53's perineal
area is excoriated.
Interview with Staff B, CNA on 4/20/2022 at 9:35 AM she stated, It is obvious no one is doing catheter care,
and the resident is upset about it.
Review of the treatment administration record (TAR) from April 1, 2022 through April 20, 2022 for pages 1-4
revealed there is no documentation of Resident #53 having been provided Foley catheter care.
Interview with the East Wing Unit Manager (UM) on 04/21/2022 at 9:22 AM the UM confirmed there is no
documentation on the TAR of Resident #53 being provided Foley catheter care.
Review of the CNA documentation flow sheet for the period of April 1, 2022 through April 20, 2022 revealed
Resident #53 received a bed bath on 4/5/2022, 4/7/2022, 4/12/2022, 4/14/2022, 4/16/2022, 4/19/2022, and
4/20/2022.
Review of the Minimum Data Set (MDS) for Resident #56 with an assessment reference date (ARD) of
2/13/2022 under Section C500 showed a Brief Interview for Mental Status (BIMS) score of 12 [cognitively
intact]. Section G for toilet use and personal hygiene was coded 3/3 requiring extensive assistance of two
person assist. Section H0100 revealed an indwelling catheter.
Review of the care plan revised on 2/14/2022 read, Resident presents as alert and oriented to person,
place, time, and situation with some occasional forgetfulness. She makes her needs known through clear
speech. Page 12 of 21 of the care plan read, Resident has an indwelling Foley catheter and is
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105613
If continuation sheet
Page 3 of 8
Printed: 05/28/2026
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
105613
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
04/21/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Live Oak Healthcare and Rehabilitation Center
1620 Helvenston St SE
Live Oak, FL 32064
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 0690
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
at risk for infection due to presence of catheter related to Neurogenic bladder. Interventions include: 1.
Assess for removal of catheter, remove when possible. Catheter and peri-care every shift and prn. Change
catheter as ordered. Observe for signs and symptoms of urinary tract infection, elevated temperature,
decreased urinary output, foul smelling urine, sediment or blood in urine. per family/resident choice.
Observe for complications that may relate to incontinence status. Staff to offer routine toileting. Staff to
provide incontinence care when episodes occur. On page 8 of 21 of the care plan it read, Resident is
incontinent of bowel and has a Foley catheter in place for neurogenic bladder. Interventions include: Assist
with toileting needs according to needs at the time. Keep clean, dry and odor free. May wear brief while in
bed.
Review of the policy and procedure titled, Urinary Catheter Care revised on November 2003 read: This
procedure may involve potential/direct exposure to blood, body fluids, infectious diseases, air contaminants,
and hazardous chemicals. Purpose: The purpose of this procedure is to prevent infection of the residents'
urinary tract.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105613
If continuation sheet
Page 4 of 8
Printed: 05/28/2026
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
105613
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
04/21/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Live Oak Healthcare and Rehabilitation Center
1620 Helvenston St SE
Live Oak, FL 32064
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** 6. An
observation on 04/18/22 at 10:19 AM showed resident #231 has a trachea [a part of your airway system]
and oxygen was being administered via trachea at 5 liters per minute.
Residents Affected - Some
An observation on 4/19/2022 at 1:45 PM of Resident #231's respiratory equipment showed the respiratory
equipment (concentrator) attached to her tracheostomy tubing, this supplies oxygen to her trachea, was not
plugged into the emergency power.
During an interview on 04/19/2022 at 3:16 PM the Director of Maintenance Staff stated, Each room in the
facility, especially the resident care area, should have an emergency red plug or an E-Plug. The facility has
not been able to identify which rooms have emergency power unless the power goes out and we are on
generator power. I have worked here since 2003 and this is how it has always been. Emergency plugs are
red in color. The oxygen concentrator machine does not require an emergency red plug. The nursing staff
would be better able to answer the question of if the tracheostomy equipment needs to be plugged into
emergency power. The Director of Maintenance stated, I do not see a red plug at all in this room.
Sometimes the light fixture has a red plug, but it is not here.
During an interview on 04/19/2022 at 3:35 PM with Staff G Licensed Practical Nurse LPN, she stated,
Residents that are receiving tracheostomy care or have ventilator care equipment are supposed to be
plugged into emergency power outlets, in the event the power goes out.
During an observation on 04/19/2022 at approximately 4:45 PM with the Unit Manager in Resident #231's
room the Unit Manager stated, I do not see a red emergency plug in this resident's room.
4. Review of Resident #50's medical record documented the resident was admitted to the facility on [DATE]
with diagnosis to include pneumonia due to Corona Virus Disease 2019 (COVID-19), personal history of
COVID and acute respiratory failure with hypoxia [a condition where you don't have enough oxygen in your
blood, but your levels of carbon dioxide are close to normal].
On 4/18/22 at 9:46 AM Resident #50 is observed sitting up in bed. There is a plastic bag observed laying
on top of the oxygen concentrator that is dated 3/8/22. The resident is observed to be without oxygen (O2).
The oxygen concentrator is next to the resident's bed and does not have tubing connected for the delivery
of oxygen. (Photographic evidence obtained).
On 4/19/22 at 8:30 AM Resident #50 is observed sitting up in bed eating breakfast. The resident is not
being administered oxygen.
On 4/19/22 at 2:48 PM Resident #50 is observed sitting up in bed. The resident is not being administered
oxygen.
Review of Resident #50's physician orders dated 2/3/22 read, Oxygen @ [at] 4 liters per minute via nasal
cannula continuously.
On 4/19/22 at 3:45 PM during an interview Staff G, Unit Manager stated the order should be change to
PRN (as needed), Resident #50 has been on room air. Staff G, stated, We should call the physician and
have the order changed to PRN.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105613
If continuation sheet
Page 5 of 8
Printed: 05/28/2026
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
105613
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
04/21/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Live Oak Healthcare and Rehabilitation Center
1620 Helvenston St SE
Live Oak, FL 32064
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
Level of Harm - Minimal harm
or potential for actual harm
5. Review of Resident #431's medical record documented the resident was admitted to the facility on
[DATE] with diagnosis to include sleep apnea [potentially serious sleep disorder in which breathing
repeatedly stops and starts], pulmonary embolism [a blood clot that travels to a lung artery] without acute
COR [pulmonary heart] Pulmonale [a condition that causes the right side of the heart to fail] and pleural
effusion [buildup of fluid between the layers of tissue that line the lungs and chest cavity].
Residents Affected - Some
On 4/18/22 at 9:51 AM Resident #431 is observed in bed with his eyes closed and breathing through his
mouth. The resident did not respond when his name was called. A continuous positive airway pressure
(CPAP) mask is observed on the floor next to the resident's urinal. (Photographic evidence obtained)
On 4/19/22 at 8:49 AM Resident #431 is observed in bed with his eyes closed and breathing through his
mouth. The CPAP mask is observed resting on the bedside table uncovered.
Review of the physician's orders for Resident #431 revealed no orders for use of a CPAP in the computer
on the medication and/or treatment record or in the resident's paper chart.
Review of the Food and Drug Administration (FDA) read, In the US [United States] CPAP devices are a
Class II medical device with possible risks .working with a healthcare provider to start and maintain CPAP
therapy is crucial. Diagnosing and treating sleep apnea can be challenging. To be successful with CPAP
therapy, you will need the expertise and support of clinicians.
During an interview conducted on 4/18/22 at 1:49 PM Resident #431 stated he uses his CPAP machine
religiously each night.
During an interview conducted on 4/19/22 at 3:33 PM with the Assistant Director of Nursing (ADON) an
observation was made of Resident #431's room. The ADON verified there was a CPAP machine at bedside.
The ADON pulled up the physician orders for Resident #431 and stated, There are no orders for Resident
#431 to use a CPAP machine.
Based on observation, interview, and record review the facility failed to ensure residents receive respiratory
care services to include safe handling, cleaning, storge, and dispensing of oxygen, consistent with
professional standards of practice for 6 of 8 sampled residents for respiratory care, Residents #2, #16, #50,
#128, #231 and #431.
Findings:
1. Review of Resident #2's medical record documented the resident was admitted to the facility on [DATE]
with a diagnosis of acute on chronic respiratory failure (a condition where not enough oxygen travels from
the lungs to the heart and other organs), chronic obstructive pulmonary disease (a group of diseases that
cause airflow blockage and breathing-related problems), congestive heart failure(a chronic condition where
the heart doesn't pump blood as well as it should), chronic atrial fibrillation (an irregular heartbeat), and
anemia (lacking enough healthy red blood cells to carry adequate oxygen to your body's tissue).
Review of the physician order dated 12/16/2021 read: Oxygen at 2l/min [liters per minute] via nasal cannula
continuously every shift for SOB [shortness of breath].
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105613
If continuation sheet
Page 6 of 8
Printed: 05/28/2026
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
105613
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
04/21/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Live Oak Healthcare and Rehabilitation Center
1620 Helvenston St SE
Live Oak, FL 32064
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
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
On 4/18/2022 at 10:04 AM Resident #2 was observed in bed with oxygen being administered at 4 liters per
minute via nasal cannula per an oxygen concentrator, with a humidification (water) bottle dated 4/13/2022
that was almost empty.
On 4/19/22 at 7:05 AM Resident #2 was observed in bed with oxygen running at 4 liters via nasal cannula
per an oxygen concentrator and the humidification bottle was empty.
On 4/20/2022 at 8:20 AM during an interview Resident #2 stated, I am not able to reach the oxygen
machine to change it, I have trouble rolling over.
On 4/20/22 at 8:30 AM during an interview Staff A, Registered Nurse (RN) stated, I see the oxygen is at 4
liters. I don't know what it is supposed to be on. I will check the orders.
On 4/20/22 at 8:40 AM during an interview Staff H, RN verified Resident #2's oxygen was on 4 liters and
should not be and that the humidification bottled dated 4/13/22 was empty.
2. Review of Resident #16's medical record documented the resident was admitted to the facility on [DATE]
with a diagnosis of chronic obstructive pulmonary disease (COPD), congestive heart failure, atrial flutter,
and anemia.
Review of the physician orders dated 5/14/2020 read: O2 [oxygen] at 2l/min liters per minute via nasal
cannula continuously every shift for COPD [chronic obstructive pulmonary disease].
On 4/19/2022 at 9:56 AM Resident #16 was observed in bed with oxygen administered at 4 liters per
minute via nasal cannula per an oxygen concentrator, with a humidification (water) bottle dated 4/13/2022
that was empty.
On 4/20/22 at 8:52 AM Resident #16 was observed being administered oxygen at 4 liters per minute per an
oxygen concentrator with the humidification bottle dated 4/13/2022 that was empty.
On 4/20/2022 at 8:53 AM during an interview Staff A, Registered Nurse (RN) stated, I see that the
concentrator is set at 4 liters. I really don't know what his rate is supposed to be. I will check the orders.
On 4/20/22 at 8:55 AM during an interview Staff H, RN verified the oxygen concentrator was administering
oxygen to the resident at 4 liters per minute via nasal cannula and the humidification bottle was empty.
On 4/20/2022 at 8:55 AM during an interview Staff H, RN stated, I expect that nurses will verify oxygen
settings at least once in the shift and change the humidification bottles when empty.
Review of the policy and procedure titled, Oxygen Safety with an approval date of 2/17/2022 read: Purpose:
The purpose of this procedure is to provide general information concerning oxygen safety and to promote
safety precautions during oxygen administration. Oxygen Administration: 1. Oxygen therapy is administered
to a resident only upon the written order of a licensed physician. Oxygen in use: 4. The humidifying jar
should be used for O2 delivery> 2lm [greater than 2 liters per minute] or unless otherwise ordered. 5.
Maintain the water level in the jar high enough so that the water bubbles as the oxygen goes through. 6. All
gauges and cylinders must be inspected before oxygen is turned on to assure that they are in proper
working order and are properly fitted.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105613
If continuation sheet
Page 7 of 8
Printed: 05/28/2026
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
105613
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
04/21/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Live Oak Healthcare and Rehabilitation Center
1620 Helvenston St SE
Live Oak, FL 32064
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
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
3. Review of Resident #128's medical record documented the resident has diagnosis to include,
pneumonia, chronic obstructive pulmonary disease (COPD), chronic kidney disease, and atrial fibrillation
(an irregular heartbeat).
Review of the physician orders dated 4/12/22 read, Ipratropium albuterol solution 0.5/2.5 (3) 3 mg
[milligrams]/3 ml [milliliters] 1 vial inhale orally every 8 hours for wheezing.
On 4/19/2022 at 8:12 AM Resident #128's passive nebulizer (a breathing machine used to inhale
medication to clear your airways or to treat infections) was observed laying on the nightstand, uncovered.
On 4/20/2022 at 7:21 AM Resident #128's passive nebulizer was observed laying on the nightstand
uncovered.
During an interview on 4/20/2022 at 1:08 PM Staff A, Registered Nurse (RN) stated, After medication
administration, the respiratory equipment should be cleaned and placed in a plastic bag.
During an interview on 4/20/22 at 1:18 PM Resident #128 stated, They give my treatment and never come
back to do anything with the nebulizer, so I have to put it on the bed or the nightstand.
Policy and Procedure titled Cleaning and servicing Nebulizers approval date of 2/17/2022 read: Procedure
guidelines: Cleaning guidelines for the mouthpiece: 1. Rinse with hot water and allow to air dry on a paper
towel before storage. 2. Store in approved containers between uses. 3. Replace tubing/mouthpiece weekly
and as needed.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105613
If continuation sheet
Page 8 of 8