FDA Adverse Event Malfunction Summary report: N

TRANSTAR STRETCHER

MDR report key: 2011992 · Received February 14, 2011

Report

Report Number
1824206-2011-00820
Event Type
Malfunction
Date Received
February 14, 2011
Date of Event
January 20, 2011
Report Date
January 20, 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 ONE GAS SPRING WAS LEAKING AND THE RELEASE PIN WAS STUCK ON THE OTHER CYLINDER. THE TECHNICIAN REPLACED BOTH GAS SPRINGS TO REPAIR THE STRETCHER.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATES THE HEAD SECTION WILL NOT LOWER TO THE FLAT POSITION.

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