F 0760
Ensure that residents are free from significant medication errors.
Level of Harm - Actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
closed resident record review, review of a facility medication error report, review of pharmacy labels, staff
interview, and policy review, the facility failed to ensure a resident was free from a significant medication
error. This affected one (#105) of three residents reviewed for medication errors. Actual Harm occurred on
09/30/25 for Resident #105, when a nurse crushed and administered an extended release Morphine
(narcotic pain medication) tablet to the resident, while also administering double the ordered dose of
prescribed Lyrica (anticonvulsant analgesic) to the resident, resulting in the need to administer Narcan
(opioid reversal agent) to the resident to reverse the effects of a drug overdose and to be evaluated at the
local emergency department (ED), after the overdose occurred. Findings include: Review of Resident
#105's medical record revealed he was admitted to the facility on [DATE]. His diagnoses included chronic
pain syndrome, opioid dependence, low back pain, Barret's Esophagus (a condition in which the lining of
the swallowing tube/ esophagus that connected the mouth to the stomach became damaged by acid reflux
causing the lining to thicken, which could result in difficulty swallowing), and adult-onset diabetes mellitus.
Review of Resident #105's significant change Minimum Data Set (MDS) assessment dated [DATE]
revealed the resident did not have any communication issues and was cognitively intact. He was not coded
as having displayed any behaviors during the 14 days of the assessment period. He was indicated on the
MDS as having received scheduled pain medication, but no pain medications had been administered on an
as needed (prn) basis. He complained of occasional pain in the past 5 days reporting having had pain that
was a three on a 1-10 pain scale that did not affect his sleep or day to day activities. The medication section
was coded to reflect he had been given opioid pain medications during the seven day assessment period.
Review of Resident #105's care plans revealed he had an active care plan in place for being at risk for pain
and known to have chronic pain related to low back pain (LBP), chronic pain syndrome, back pain, wounds
right hip, and taking opioids. The care plan was initiated on 03/26/24 and was last revised on 09/19/25. The
goal was for the resident to verbalize adequate relief of his pain or the ability to cope with incompletely
relieved pain. The interventions included administering medications as ordered, observe for ineffectiveness
and side effects of pain medication (confusion. hallucinations etc.), and report abnormal findings to the
physician. Review of Resident #105's physician's orders revealed the resident had an order to receive MS
Contin (an extended release, opioid medication used for the long-term, around the clock management of
severe pain) Extended Release (ER) 15 milligrams (mg) by mouth (po) twice a day for chronic pain. The
order originated on 09/26/25 and continued until 10/01/25, when the order was altered to reflect the
additional directive to Do Not Crush the medication. The resident also had an order to receive Lyrica (an
anti-convulsant medication used to treat nerve pain from various conditions) 150 mg po three times a day
for neuropathy pain. That order had recently been re-ordered as of 09/28/25. The physician's orders did not
provide any directive allowing staff to crush medications as needed. Review of Resident
Residents Affected - Few
(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 5
Event ID:
365466
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
365466
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/20/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
The Laurels of Heath
717 South 30th Street
Heath, OH 43056
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 0760
Level of Harm - Actual harm
Residents Affected - Few
#105's progress notes revealed the resident was sent out to the hospital on [DATE] for worsening of the
pressure ulcer to his coccyx. The wound had an increase in size, an increase in pain, and an increase in
purulent drainage with a foul odor. He returned to the facility on [DATE] on intravenous antibiotics and a new
order for MS Contin 15 mg po twice a day for pain. He did not return with an order for the use of Lyrica 150
mg po three times a day that had been ordered prior to his transfer to the hospital on [DATE]. Review of a
telehealth note dated 09/28/25 at 8:00 A.M. revealed the nurse practitioner was notified by nursing that
Resident #105's previously prescribed Lyrica that was ordered at 150 mg po three times a day for
neuropathy was not on the hospital's discharge summary upon his return to the facility on [DATE]. The
resident was requesting his Lyrica to be re-instated for pain. An order was given for Lyrica 150 mg po three
times a day to be given on a scheduled basis with directions to hold for sedation. Review of a nurse's
progress note from registered nurse (RN) #100 on 09/30/25 at 4:45 P.M. revealed a nurse had alerted her
that Resident #105 had confusion and was showing slight sedation effects. The resident was noted to be
oriented to self and place when assessed by RN #100 with the following vital signs: Blood pressure 95/75,
pulse 65 beats per minute, respirations at 17/ minute, and a temperature of 98 degrees Fahrenheit. The
resident's oxygen level was normal at 95% on room air. The nurse reviewed the resident's medication and
reported he received an extra dose of medication (not specified) and his extended-release medication (not
specified) was given crushed with his other scheduled medications. The physician's assistant (PA) was
notified immediately regarding the resident's current assessment findings and his reported vital signs. A
new order was received to administer Narcan ((an opioid antagonist medication used to reverse or reduce
the effects of opioids) 4 mg/ 0.1 milliliters (ml) nasal spray x 1 dose. Review of a nurse's progress note by
RN #100 dated 09/30/25 at 4:51 P.M. revealed a new order was received to hold Resident #105's evening
dose of MS Contin and Lyrica per an order from the PA. Resident #105 was re-assessed, and his blood
pressure was 111/67, pulse 67, respirations of 17, and his oxygen level was 97% on room air. The resident
was noted to be alert and oriented to person, place, time, and event. His wife that was visiting wanted him
to go to ER to be assessed. The PA was notified and gave an order for the resident to be transferred to the
ER for an evaluation as requested by the resident's family. It was deemed by the PA to be a non-emergent
transport, due to the resident's current orientation, alertness, and ability to eat and drink. It was made
known to the PA and the wife that the community's ambulette service could not transport the resident to the
hospital for a couple of hours and both were in agreement that the resident did not need transported
emergently and could wait for the ambulette to be available for transport. The resident returned to the
facility on [DATE] at 2:10 A.M. in stable condition. He was alert and oriented upon his return and aroused/
responded appropriately. He did not return with any new orders. Review of Resident #105's medication
administration record (MAR) for September 2025 revealed the resident was scheduled to receive his MS
Contin 15 mg ER tablet po twice a day at 8:00 A.M. and 8:00 P.M. He received his dose of MS Contin 15
mg ER the morning of 09/30/25 at 8:00 A.M. He also received his ordered dose of Lyrica 150 mg at 8:00
A.M., as was ordered three times a day. Review of Resident #105's hospital records for his ER visit on
09/30/25 revealed they included an emergency department (ED) note dated 09/30/25 at 8:18 P.M. that
indicated the resident's chief complaint was identified as presenting with a drug overdose. He was being
evaluated for hallucinations and an altered mental status after receiving a crushed up Morphine ER tablet
at the nursing facility according to his wife that accompanied him to the ER. Upon his arrival, the resident
reported he was at his baseline and denied any current complaints. He requested to be sent back to the
nursing facility at that time. His symptoms were likely due to receiving a crushed extended release
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365466
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
365466
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/20/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
The Laurels of Heath
717 South 30th Street
Heath, OH 43056
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 0760
Level of Harm - Actual harm
Residents Affected - Few
Morphine tablet as his symptoms were currently resolved. No medication changes were made as a result of
his ER visit. Review of Resident #105's pharmacy label for the MS Contin (Morphine ER) 15 mg tablets
revealed the label on a Controlled Drug Receipt/ Record/ Disposition form dated 09/28/25 included
instructions to the nurse that read Do Not Crush, Chew, or Split the medication tablet. The label on the
blister pack for the MS Contin 15 mg tablets also included the same instructions not to crush, chew, or split
the tablets. Review of a Medication and Treatment Incident Report dated 09/30/25 (date of incident/ date
discovered/ and date reported) completed by RN #100 revealed Resident #105 was given MS Contin ER
oral tablet crushed, despite it being an extended-release tablet. The time of the incident was indicated to be
4:45 P.M. The medication error resulted in the need for medical treatment/ intervention, as the resident was
given Narcan x 1. The medication error was determined to be the result of the nurse's failure to follow
procedure. The corrective action taken included providing additional training and written counseling. The
training provided involved crushable versus non-crushable medication. The nurse involved in the medication
error was not identified by name on the incident report. The medication and treatment incident report did
not mention anything about the resident receiving an extra dose of any medication, as was indicated in the
progress note dated 09/30/25 at 4:45 P.M., only that his MS Contin had been given crushed with his other
medications. Review of the nursing schedule for 09/30/25 revealed licensed practical nurse (LPN) #150 was
the nurse assigned to work Resident #105's hall at the time the significant medication error occurred on the
resident. Certified Nursing Assistant (CNA) #200 was one of three CNA's that was assigned to work
Resident #105's hall when the medication error occurred. Review of the employee file for LPN #150
revealed he received a final written warning on 09/30/25, as a result of the significant medication error that
he committed on Resident #105. The disciplinary action given with the final warning was for an infraction of
work Rule # 20. A description of the reason for the disciplinary action indicated the nurse committed a
medication error that resulted in a resident being sent to the ER to be evaluated following the error.
Education was provided to the nurse on medications that could not be crushed, i.e. extended release
medications. The nurse signed the disciplinary action report on 10/06/25. On 10/16/25 at 1:12 P.M., an
interview with LPN #150 via phone confirmed he did work on 09/30/25, when Resident #105's medication
error pertaining to his MS Contin and Lyrica occurred. He further confirmed he was the nurse that
administered Resident #105's 8:00 A.M. medications to him. He indicated they just added a new medication
for Resident #105's pain control, as his pain medication was changed to Morphine ER. He admitted to
crushing the MS Contin (Morphine) ER tablet along with all other medications he gave to the resident that
morning. He denied he was aware the MS Contin was not to be crushed. That was the first time he had
worked with the resident, since the MS Contin had been ordered. He claimed he had interacted with the
resident that entire day following the administration of his morning medications. He reported the resident
had been having a change in his condition, as his overall health had been declining. He recalled the
resident was pointing and speaking to things that were not there. He told the unit manager and documented
his findings. He thought it was somewhere between 10:00 A.M. and 11:00 A.M., when that occurred. The
unit manager told him she would call the resident's wife. The wife showed up at the facility later that day and
was told the resident was having lots of problems. The wife asked if they had crushed the resident's
medications. When told that they had, the wife informed him that the resident was receiving MS Contin XR
that should not be crushed. He then reported it to the unit manager. He confirmed, after that incident, he
was given a written warning, as a result of that significant medication error. He denied there was any
instructions provided with the order for the MS Contin that directed them not to crush, when he gave the
medication. He had
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365466
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
365466
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/20/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
The Laurels of Heath
717 South 30th Street
Heath, OH 43056
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 0760
Level of Harm - Actual harm
Residents Affected - Few
since been educated on what medications could and could not be crushed. On 10/16/25 at 1:43 P.M., an
interview with CNA #200 confirmed she was one of the three aides that worked on 09/30/25, when the
medication error involving Resident #105 occurred. She was not aware that a medication error had
occurred but did interact with the resident that day. She recalled the resident was very tired that day. She
helped the nurse (LPN #150) do the resident's wound treatment that day around 3:00 P.M. or 3:30 P.M. She
stated the resident was very confused and was not alert that day per his usual self. They also had to help
feed him that day, as the resident was spilling food on himself. She too reported the resident's health had
been declining and he was on hospice at that time. She recalled being at the nurses' station at the time
when the resident's wife came in and was upset with how the resident was. She thought that was around
5:30 P.M. (towards the end of her shift), but then recalled they were passing meal trays around that time, so
it could have been anywhere between 4:45 P.M. and 5:30 P.M. On 10/16/25 at 1:49 P.M., an interview with
RN #100 revealed she was the unit manager for Resident #105's hall. She described Resident #105's
normal mental status as being alert, but he could have some confusion at times. He was oriented to self
and place. He was also known to be drowsy at times, due to the medications he took and his overall health
status. She reported the nurse (LPN #150) came to her late in the afternoon of 09/30/25, and told her
Resident #105 was not feeling good. She went to his room to assess him and found the resident to be
drowsy and more confused than normal for him. She came back into her office to call the resident's provider
to inform them of the resident's noted change in condition. LPN #150 then returned to her office and
informed her that he crushed the resident's MS Contin and gave him too much Lyrica. She was asked to
clarify the nurse's note she wrote that was dated 09/30/25 at 4:45 P.M., which indicated the resident
received an extra dose of medication, in addition to his extended-release medication being crushed with
other scheduled medications. She confirmed Resident #105 was also given double the dose of Lyrica (300
mg) that was ordered for him on 09/30/25 at 8:00 A.M. She confirmed he received 300 mg, when he should
have only been given 150 mg as ordered three times a day. She indicated at the time, they had been giving
the resident a 100 mg capsule and a 50 mg capsule of Lyrica to equal a total dose of 150 mg. They then
received Lyrica 150 mg capsules from their pharmacy. LPN #150 had indicated to her that he gave
Resident #105 a 100 mg capsule of Lyrica, a 50 mg capsule of Lyrica, and a 150 mg capsule of Lyrica
equaling 300 mg (doubling his ordered dose). She was asked if the resident had been receiving his
medications crushed, prior to the incident occurring on 09/30/25. They were giving him his medications
whole in pudding, but at some point started crushing some of his medications due to him having some
swallowing issues with the larger pills. She had heard other nurses inform the resident in the past that there
were certain medications he received that they could not crush. She was not aware of any of the other
nurses ever crushing his MS Contin, prior to or after the incident on 09/30/25. She was not aware of the
nurse crushing all the resident's medications that morning and believed the resident had a standing order in
place that they could crush allowable medications. She later reported that the standing order giving them
permission to crush allowable medications had been inadvertently discontinued somewhere along the way
and was not part of his current physician's orders. She was asked if extended release or delayed release
medications could be crushed and she replied no. If there was a resident with those type of medications
ordered that were having trouble swallowing the tablet or capsule, they should reach out to the physician to
see about getting other similar medications ordered that could be given in a form the resident was able to
safely take. She confirmed they provided education to the nurses following the occurrence of that
medication error about being mindful to follow the instructions on medications' labels regarding those
medications that could not be crushed. They have
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365466
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
365466
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/20/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
The Laurels of Heath
717 South 30th Street
Heath, OH 43056
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 0760
Level of Harm - Actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
since placed a list of medications that should not be crushed on all units accessible to the nurses
administering medications. LPN #150 was the one that administered Narcan to Resident #105, after she
got the order when calling the provider. She stated within 60 seconds of receiving the Narcan, the resident
was talking per his usual. He was alert, drinking, and eating supper. The wife wanted the resident sent to
the ER, despite the resident saying he felt fine. They sent him to the ER as requested by the family and as
agreed to by the resident. He returned a short time later with no new orders. On 10/16/25 at 2:10 P.M., an
interview with facility's Director of Nursing (DON) revealed RN #100 was in the building when the
medication error involving Resident #105 on 09/30/25 occurred. She was informed there had been a
change in Resident #105's condition, which included confusion. When RN #100 was looking into the
resident's change in condition, LPN #150 said Oh my God, I crushed his Morphine. RN #100 had reached
out to the resident's provider and got an order for Narcan. Resident #105 had positive results to the Narcan
and was back to his baseline. His wife wanted him sent out to the ER anyway. He was found to be at
baseline when he was evaluated at the hospital. She confirmed she was the one that completed the
medication error report the day after the medication error occurred. She spoke with the unit manager (RN
#100), pulled the nurse's documentation, reviewed the progress notes, and talked with the PA, as part of
her review. She stated they started crushing Resident #105's medications ever since he had thyroid
surgery, but not all of his medications. She was not 100% sure if all his medications had been crushed that
morning, or if it was just the MS Contin. She confirmed the MS Contin should not be crushed as it was an
extended-release tablet and would result in the resident receiving an immediate dose of Morphine 15 mg
instead of it being slowly released over a 12 hour period. Review of the facility's Medication Administration
policy revised 10/17/23 revealed resident medications were to be administered in an accurate and safe
manner. Medications were to be administered in accordance with written orders of the attending physician.
The nurse was to check the Do Not Crush list before crushing medications. If necessary, the nurse was to
contact the ordering physician for a change to a different route of administration when the medication could
not be crushed. This deficiency represents non-compliance investigated under Complaint Number
2637682.
Event ID:
Facility ID:
365466
If continuation sheet
Page 5 of 5