FDA Adverse Event Malfunction Summary report: N

TRANSTAR STRETCHER

MDR report key: 2253395 · Received August 3, 2011

Report

Report Number
1824206-2011-04102
Event Type
Malfunction
Date Received
August 3, 2011
Date of Event
July 25, 2011
Report Date
July 25, 2011
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

TECH FOUND THE BED IN THE HALLWAY NEAR THE E.R. THE BRAKES DO NOT HOLD WHEN SET, THE CASTERS ROTATE TO THE SIDE. REPLACED THE 4 BRAKE CASTERS TO RESOLVE THIS ISSUE.

Description of Event or Problem · 1

BED WAS FOUND IN THE HALLWAY NEAR THE E.R. THE BRAKES DO NOT HOLD WHEN SET, THE CASTERS ROTATE TO THE SIDE. NO INJURY REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM INC. P8000

Patients

Seq Age Sex Outcome Treatment
1