FDA Adverse Event Malfunction Summary report: N

TRANSTAR STRETCHER

MDR report key: 1800764 · Received August 4, 2010

Report

Report Number
1824206-2010-09150
Event Type
Malfunction
Date Received
August 4, 2010
Date of Event
July 12, 2010
Report Date
July 12, 2010
Manufacturer
HILL-ROM, INC.
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CO, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN REPLACED THE WORN BRAKE CASTER TO REPAIR THE STRETCHER.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATES THE CASTER WOULD LOCK AND HOLD BUT PRESSURE ON SIDE OF THE CASTER WOULD CAUSE IT TO SWIVEL.

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