FDA Adverse Event Death Summary report: N

3000 ELECTRIC - 78"

MDR report key: 1575090 · Received January 8, 2010

Report

Report Number
9680128-2010-00001
Event Type
Death
Date Received
January 8, 2010
Date of Event
August 1, 2009
Report Date
December 11, 2009
Manufacturer
STRYKER MEDICAL QUEBEC, LP
Product Code
FNL
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

IT WAS REPORTED, THROUGH A NEWSPAPER ARTICLE, THAT A PATIENT WAS FOUND DEAD BY NURSE IN 2009. IT WAS REPORTED THAT THE NURSE FOUND THE PATIENT WITH HIS HEAD STUCK BETWEEN THE LEFT SIDERAIL AND THE FOOT BOARD. IT WAS REPORTED THAT THE PATIENT WAS FOUND WITH RED MARKS AROUND HIS NECK AND CHEST AREA, AND IT WAS DETERMINED THAT THE PATIENT HAD BEEN DEAD FOR A WHILE, SO NO RESUSCITATION ATTEMPTS WERE MADE. FINALLY, IT WAS REPORTED THAT THE (NON-STRYKER) MOVEMENT MONITORING ALARM HAD BEEN UNPLUGGED BY THE HOSPITAL STAFF OR THE PATIENT HIMSELF.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 3000 ELECTRIC - 78" HOSPITAL BED, A-C POWERED, ADJUSTABLE FNL STRYKER MEDICAL QUEBEC, LP FL13E78 NA

Patients

Seq Age Sex Outcome Treatment
1 UNK Death