FDA Adverse Event Summary report: N

IN TOUCH EU

MDR report key: 1930010 · Received November 19, 2010

Report

Report Number
9680128-2010-00317
Date Received
November 19, 2010
Date of Event
October 25, 2010
Report Date
October 25, 2010
Manufacturer
STRYKER MEDICAL QUEBEC, LP
Product Code
FNL
Report Source
Manufacturer report
Reporter Location
NC, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE BED HAD NO POWER. NO INJURY REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 IN TOUCH EU HOSPITAL BED, A-C POWERED, ADJUSTABLE FNL STRYKER MEDICAL QUEBEC, LP 2131000000 NA

Patients

Seq Age Sex Outcome Treatment
1 UNK