FDA Adverse Event Malfunction Summary report: N

ELECTRIC MED/SURG BED

MDR report key: 2964301 · Received February 15, 2013

Report

Report Number
0001831750-2013-01245
Event Type
Malfunction
Date Received
February 15, 2013
Date of Event
January 22, 2013
Report Date
January 22, 2013
Manufacturer
STRYKER MEDICAL-KALAMAZOO
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

IT WAS REPORTED THAT THE BRAKES WERE NOT HOLDING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
67965 ELECTRIC MED/SURG BED BED, AC-POWERED ADJUSTABLE HOSPITAL FNL STRYKER MEDICAL-KALAMAZOO

Patients

Seq Age Sex Outcome Treatment
1