FDA Adverse Event Malfunction Summary report: N

TRANSTAR STRETCHER

MDR report key: 2094026 · Received April 20, 2011

Report

Report Number
1824206-2011-02285
Event Type
Malfunction
Date Received
April 20, 2011
Date of Event
March 21, 2011
Report Date
March 21, 2011
Manufacturer
HILL-ROM, INC.
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN FOUND THE BRAKE/STEER LINKAGES AT BOTH ENDS OF THE STRETCHER WERE NOT FUNCTIONING. HE USED A BRAKE/STEER UPGRADE TO REPAIR THE STRETCHER.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATES THE CASTERS ARE NOT HOLDING.

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