FDA Adverse Event Malfunction Summary report: N

LIT GOBED BNQ

MDR report key: 2091148 · Received April 20, 2011

Report

Report Number
1831750-2011-03770
Event Type
Malfunction
Date Received
April 20, 2011
Date of Event
March 25, 2011
Report Date
March 25, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

IT WAS REPORTED THAT THE HEAD RIGHT CASTER HORN SHAFT WAS BROKEN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 LIT GOBED BNQ A/C HOSPITAL BED FNL STRYKER MEDICAL FL23 NA

Patients

Seq Age Sex Outcome Treatment
1 UNK