FDA Adverse Event Malfunction Summary report: N

TRANSTAR STRETCHER

MDR report key: 1993229 · Received January 21, 2011

Report

Report Number
1824206-2011-00380
Event Type
Malfunction
Date Received
January 21, 2011
Date of Event
December 30, 2010
Report Date
December 30, 2010
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

TECHNICIAN FOUND THE BRAKE HARDWARE WAS WORN OUT DUE TO NORMAL WEAR AND TEAR. THE TECHNICIAN REPLACED THE BRAKE HARDWARE TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

TECHNICIAN ALLEGED THAT THE BRAKES ARE NOT HOLDING. NO ONE WAS HURT OR INJURED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TRANSTAR STRETCHER A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 8050

Patients

Seq Age Sex Outcome Treatment
1