FDA Adverse Event Malfunction Summary report: N

TRAUMA STRETCHER

MDR report key: 1898828 · Received November 8, 2010

Report

Report Number
1831750-2010-03571
Event Type
Malfunction
Date Received
November 8, 2010
Date of Event
October 12, 2010
Report Date
October 12, 2010
Manufacturer
STRYKER CORP, MED DIV
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE TOP RAIL ON THE LEFT SIDERAIL IS BROKEN IN HALF AND THE FOOT END JACK IS DRIFTING. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TRAUMA STRETCHER HOSPITAL WHEELED STRETCHER FPO STRYKER CORP, MED DIV 1020 NA

Patients

Seq Age Sex Outcome Treatment
1 NA