FDA Adverse Event Malfunction Summary report: N

TRANSTAR STRETCHER

MDR report key: 1901107 · Received November 10, 2010

Report

Report Number
1824206-2010-10963
Event Type
Malfunction
Date Received
November 10, 2010
Date of Event
October 17, 2010
Report Date
October 17, 2010
Manufacturer
HILL-ROM, INC.
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN FOUND THE BRAKE/STEER MECHANISM LINKAGE WAS BROKEN. HE USED A BRAKE/STEER UPGRADE TO REPAIR THE BED.

Description of Event or Problem · 1

INFO RECEIVED INDICATES THE BRAKE/STEER IS NOT WORKING. THE TECHNICIAN FOUND WHEN HE ENGAGED THE BRAKE PEDAL; THE CASTERS DID NOT LOCK IN BRAKE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM, INC. 8000

Patients

Seq Age Sex Outcome Treatment
1