FDA Adverse Event Malfunction Summary report: N

IN TOUCH

MDR report key: 1082037 · Received July 21, 2008

Report

Report Number
9680128-2008-00048
Event Type
Malfunction
Date Received
July 21, 2008
Date of Event
June 24, 2008
Report Date
June 24, 2008
Manufacturer
STRYKER MEDICAL QUEBEC LP
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

IT WAS REPORTED THAT THE BED WOULD NOT MOVE OUT OF THE HIGHEST POSITION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 IN TOUCH HOSPITAL BED, A-C POWERED, ADJUSTABLE FNL STRYKER MEDICAL QUEBEC LP 2130000000 NA

Patients

Seq Age Sex Outcome Treatment
1 UNK