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.
Based on observation, interviews and records review, the facility failed to develop a person-centered
individualized care plan for 1 of 8 sampled residents (Resident 7.) This failure had the potential for facility
staff to not provide adequate care to Resident 7's eyes which could cause further damage to his eyes
and/or blindness.
Findings:
During on observation on 8/13/24 at 10:25 a.m., in Resident 7's room, Resident 7 had his right eye covered
with a gauze dressing. Resident 7's left eye was open and seemed to be looking at the HFEN.
During an interview on 8/13/24 at 2:57 p.m., Licensed Nurse C stated Resident 7 has his eye covered
because his medical condition causes the eye to be swollen preventing the eye lids from closing. He got
eye drops and the dressing to prevent his eye from drying out.
During an interview and concurrent record review on 8/14/24 at 3:35 p.m., Licensed Nurse C reviewed the
electronic care plan for Resident 7, and it was determined that an individualized care plan concerning
Resident 7's vision had not been written.
The facilities policy Person-Centered Care Plan, dated 8/2024, indicated a Person-Centered Care Plan will
be written for each resident. The plan will be based on the medical, functional, and psychosocial needs of
the resident and will include instructions for providing effective and person-centered care that meets the
professional standards of quality care.
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 5
Event ID:
555590
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
555590
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/16/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Healdsburg Hospital D/P Snf
1375 University Avenue
Healdsburg, CA 95448
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 0755
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Provide pharmaceutical services to meet the needs of each resident and employ or obtain the services of a
licensed pharmacist.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, and record review, the facility failed to ensure professional standards of practice
when two of three residents (Resident 16 and Resident 5) did not have their enteral tube (a soft, flexible
tube which enters a surgically created opening in the abdominal wall and is used to administer food, fluids,
and medications to a person that cannot receive food, fluid, or medications through their mouth) flushed
(the process of gently pushing water through the tube to clean it) before and after medication
administration. This failure had the potential to cause a blockage in the enteral tube and delay the
administration of critical medications (priority medications that should not be omitted or delayed).
Findings:
Record review of a document titled, Face Sheet (resident demographics) for Resident 16, indicated
Resident 16 was admitted to the facility on [DATE].
Record review of a document titled, Problem List for Resident 16, indicated Resident 16 had the following
diagnoses: traumatic brain injury with prolonged (more than 24 hours) loss of consciousness without return
to pre-existing conscious level, encounter for PEG (percutaneous endoscopic gastrostomy [the procedure
to insert an enteral tube into the abdomen]), fecal incontinence (loss of conscious control over bowel
movements), and gastroesophageal reflux disease (GERD - a condition in which stomach acid repeatedly
flows back up into the tube connecting the mouth and stomach, called the esophagus).
During an observation on 8/14/24 at 10:32 AM, Licensed Nurse A prepared and administered the following
medications through an enteral tube to Resident 16:
Docusate 100 Milligrams (mg - a unit of weight measure), three liquid packets of 10 milliliters (ml - a unit of
liquid measure) each (a medication used to prevent or treat constipation [a blockage and/or hardening of
stool in the intestinal tract]).
Senna 8.6 mg, one tablet (a medication used to prevent constipation).
Famotidine 20 mg, one tablet (a medication used to treat stomach ulcers, heartburn, acid indigestion, and
gastroesophageal reflux disease).
Gabapentin 300 mg, one capsule (a medication used to treat or prevent seizures [a sudden, uncontrolled
burst of electrical activity in the brain that can cause temporary changes in muscle tone, behavior,
sensations, or awareness] or to treat nerve pain).
Potassium Chloride 1.5 grams (gm - a unit of weight measure), mixed with 15 ml of water (a medication
used in the management and treatment of hypokalemia [a condition where potassium [an important
chemical in the body] levels are too low in the blood]).
Polyethylene Glycol (PEG) 17 gm, mixed with enough water to dissolve the powder (a medication used to
prevent constipation).
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555590
If continuation sheet
Page 2 of 5
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
555590
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/16/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Healdsburg Hospital D/P Snf
1375 University Avenue
Healdsburg, CA 95448
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 0755
Level of Harm - Minimal harm
or potential for actual harm
Licensed Nurse A administered each medication separately and flushed Resident 16's enteral tube with a
small amount of water (approximately 5 ml) between each medication.
Licensed Nurse A did not flush the enteral tube before administering medications to Resident 16. Licensed
Nurse A did not flush the enteral tube after administering medications to Resident 16.
Residents Affected - Few
During an interview on 8/14/24 at 11:25 AM, Licensed Nurse A stated she flushed Resident 16's enteral
tube with approximately 5 ml of water between each medication administered through the enteral tube.
Record review of a document titled, Face Sheet (resident demographics) for Resident 5, indicated Resident
5 was admitted to the facility on [DATE].
Record review of a document titled, Problem List for Resident 5, indicated Resident 5 had the following
diagnoses: traumatic brain injury (TBI - A traumatic brain injury refers to a brain injury that is caused by an
outside force. TBI can be caused by a forceful bump, blow, or jolt to the head or body, or from an object
entering the brain), seizure disorder, encounter for PEG, abdominal distension (abdomen is measurably
swollen beyond its normal size, often due to trapped gas), and pneumonia (an infection that inflames air
sacs in one or both lungs, which may fill with fluid.)
During an observation on 8/14/24 at 12:39 PM, Licensed Nurse A prepared and administered the following
medications through an enteral tube for Resident 5:
Simethicone 125 mg, one tablet (a medication used to treat excessive gas in the digestive tract).
Clonazepam 0.5 mg, four tablets (a medication used to treat seizure disorders and anxiety disorders [A
mental health disorder characterized by feelings of worry, anxiety, or fear that are strong enough to interfere
with one's daily activities]).
Oxycodone 5 mg, one tablet (a medication used to treat pain).
Milk of Magnesia (MOM) 5ml (a medication used as a dietary supplement of magnesium [an important
chemical in the body]).
Levetiracetam, 1500ml (a medication used to treat seizure disorders).
Licensed Nurse A administered each medication separately and flushed Resident 5's enteral tube with a
small amount of water (approximately 5 ml) between each medication.
Licensed Nurse A did not flush the enteral tube before administering medications to Resident 5. Licensed
Nurse A did not flush the enteral tube after administering medications to Resident 5.
During an interview on 8/14/24 at 4:03 PM, the Director of Nursing (DON) stated the facility policy was to
always flush before and after enteral tube medication administration. The DON further stated the policy
specified a minimum flush of 15 ml of water before and after medication administration through an enteral
tube.
Record review of a Policy and Procedure titled, Medication Administration Through a Feeding Tube, last
approved on 3/2021, indicated flush feeding tube with 15-30 ml of warm water before
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555590
If continuation sheet
Page 3 of 5
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
555590
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/16/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Healdsburg Hospital D/P Snf
1375 University Avenue
Healdsburg, CA 95448
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 0755
administering medications. The Policy and Procedure further indicated flush the feeding tube with at least
15 - 30 ml of warm water after the completion of the medication administration.
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:
555590
If continuation sheet
Page 4 of 5
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
555590
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/16/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Healdsburg Hospital D/P Snf
1375 University Avenue
Healdsburg, CA 95448
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 - Some
Procure food from sources approved or considered satisfactory and store, prepare, distribute and serve
food in accordance with professional standards.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation and interview and facility policy review, the facility failed to ensure food items were stored in a
manner that complied with food handling practices to prevent food-borne illness (illness caused by the
ingestion of contaminated food or beverages), when two bowls of prepared food were in the walk-in
refrigerator without any labeling and several food items were opened and without labels in the dry storage
area. This failure had the potential to result in the rapid growth of pathogenic (capable of causing disease)
microorganisms (e. g. bacteria, virus etc.) that could cause food-borne illnesses and could affect the
residents of the facility.
Findings:
During an observation on 8/12/24 at 9:15 a.m., food items in the freezers were labeled with the arrival date.
Food items in the refrigerators had the arrival date. Food items in dry storage were labeled with the arrival
date.
On 8/14/24 at 9:30 a.m., during an observation in the dry storage area, several open food packages were
found without a label, starting with a large open box that contained the oatmeal in plastic bag, but no label.
An open box of Nilla wafers, 1 bag of tortilla chips, an 8-ounce box of pasta and a box of pancake mix had
been opened and partially used but were without labels to show an opened date or use by date.
During an interview on 8/14/24 at 9:45 a.m., Kitchen Staff E stated that upon delivery, the items were
labeled with a Received Date. The boxes and bags of the food products taken out of the shipping boxes
also get the Received Date. When the food packages are opened, they should have a new label that
showed the date received, date opened and a use by date.
During an observation on 8/14/24 at 9:50 a.m., the walk-in refrigerator was found to have open items
unlabeled. One item was a bowl of cooked and cut up chicken, covered with plastic wrap. No label was
found. The second item was a dark colored sauce in a bowl, covered in plastic wrap and not labeled.
During an observation and concurrent interview on 8/14/24 at 9:53 a.m., Kitchen Staff D removed the items
and stated there should be labels that include the received date, open date, and use by date. Kitchen Staff
D stated staff could generate labels electronically. Kitchen Staff D stated he would need to talk with staff.
The facilities policy and procedure titled Food and Supply Storage, dated 6/2023, indicated: Cover, label
and date unused portions and open packages. Complete all sections of the [NAME] orange label or other
approved labeling system. The policy is to store food items and supplies in such a manner as to prevent
contamination to maintain the safety and wholesomeness of the food for human consumption.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555590
If continuation sheet
Page 5 of 5