FDA Adverse Event
Injury
Summary report: N
ENDURA GLIDER
MDR report key: 211615
·
Received February 23, 1999
Report
- Report Number
- 211615
- Event Type
- Injury
- Date Received
- February 23, 1999
- Date of Event
- February 15, 1999
- Report Date
- February 22, 1999
- Manufacturer
- UNK
- Product Code
- KNL
- Adverse Event
- Yes
- Report Source
- User Facility report
- Reporter Location
- KY, US
- Reporter Occupation
- RISK MANAGER
Narratives
Description of Event or Problem · 1
A 43-YEAR-OLD MALE PATIENT ATTEMPTED SUICIDE BY HANGING SELF ON BATHROOM DOORKNOB ON PSYCH UNIT, USING A BLACK STRAP. THE STRAP APPEARS TO BE IDENTICAL TO THE STRAPS WHICH ARE TIED TO THE ENDURA GLIDER TRANSPORT BOARDS IN THE RADIOLOGHY DEPT. THE PATIENT HAD BEEN TO RADIOLOGY FOR X-RAYS ON THE MORNING OF THE SUICIDE ATTEMPT. WHEN THE PATIENT WAS FOUND, THERE WAS A PULSE BUT NO RESPIRATIONS. CARDIOPULMONARY RESUSCITATION STARTED, AND PATIENT BEGAN SPONTANEOUS RESPIRATIONS. PATIENT WAS ADMITTED TO CARDIAC CARE UNIT, AND ON A VENTILATOR UNTIL 2/19/99 WHEN HE WAS REMOVED FROM VENTILATORY AND BREATING ON HIS OWN.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ENDURA GLIDER | TRANSPORT BOARD | KNL | UNK | UNK | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 44 YR | Hospitalization| L | MEDICATIONS: HALDOL, ATIVAN, COGENTIN, NICOTINE| PATCH. |