FDA Adverse Event Malfunction Summary report: N

TRANSTAR STRETCHER

MDR report key: 1800730 · Received August 4, 2010

Report

Report Number
1824206-2010-09154
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
TX, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN FOUND THE HYDRAULIC CYLINDER WAS NOT HOLDING IN THE HIGH POSITION. THE TECHNICIAN REPLACED THE FOOT END HYDRAULIC CYLINDER TO REPAIR THE STRETCHER.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATES THE FOOT HI/LOW IS GOING DOWN BY ITSELF.

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