FDA Adverse Event Malfunction Summary report: N

TRANSTAR STRETCHER

MDR report key: 2130305 · Received May 9, 2011

Report

Report Number
1824206-2011-02620
Event Type
Malfunction
Date Received
May 9, 2011
Date of Event
April 17, 2011
Report Date
April 17, 2011
Manufacturer
HILL-ROM, INC.
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECH FOUND THE CASTERS WERE WORN AND OLD. HE REPLACED THE FOUR CASTERS TO REPAIR THE STRETCHER.

Description of Event or Problem · 1

INFO RECEIVED INDICATES THE BRAKE WILL NOT HOLD. THE CASTERS CONTINUE TO MOVE FROM SIDE TO SIDE WHEN THE BRAKE IS ENGAGED.

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