FDA Adverse Event Malfunction Summary report: N

TRANSTAR STRETCHER

MDR report key: 1850110 · Received September 28, 2010

Report

Report Number
1824206-2010-10159
Event Type
Malfunction
Date Received
September 28, 2010
Date of Event
September 1, 2010
Report Date
September 1, 2010
Manufacturer
HILL-ROM INC.
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN FOUND THE BOLT AND NUT MISSING FROM THE HEX ROD SHOULDER LINKAGE. THE TECHNICIAN REPLACED THE NUT AND BOLT TO REPAIR THE STRETCHER.

Description of Event or Problem · 1

INFO RECEIVED INDICATES, THE BRAKE/STEER CASTER IS NOT HOLDING WHEN 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