FDA Adverse Event Malfunction Summary report: N

TRANSTAR STRETCHER

MDR report key: 2241334 · Received September 2, 2011

Report

Report Number
1824206-2011-04627
Event Type
Malfunction
Date Received
September 2, 2011
Date of Event
August 22, 2011
Report Date
August 22, 2011
Manufacturer
HILL-ROM INC.
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CO, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN REPLACED THE CASTER TO REPAIR THE STRETCHER.

Description of Event or Problem · 1

INFO RECEIVED INDICATES THE BRAKE CASTER WHEEL WILL LOCK WHEN THE BRAKE IS SET, BUT THE CASTER WOULD ROTATE IF PUSHED ON FROM THE SIDE OF THE STRETCHER.

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