FDA Adverse Event Malfunction Summary report: N

ADVANTAGE SERIES 29

MDR report key: 2574247 · Received May 7, 2012

Report

Report Number
1831750-2012-04896
Event Type
Malfunction
Date Received
May 7, 2012
Date of Event
April 8, 2012
Report Date
April 8, 2012
Manufacturer
STRYKER MEDICAL
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE HEAD JACK WAS DRIFTING AND THE FOOT END COVER WAS BROKEN WITH SHARP EDGES EXPOSED. NO PATIENT INVOLVEMENT OAR ADVERSE CONSEQUENCES WERE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ADVANTAGE SERIES 29 HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1509 NA

Patients

Seq Age Sex Outcome Treatment
1