FDA Adverse Event Malfunction Summary report: N

GPS PROCEDURAL STRETCHER

MDR report key: 1934260 · Received December 3, 2010

Report

Report Number
1824206-2010-11370
Event Type
Malfunction
Date Received
December 3, 2010
Date of Event
November 8, 2010
Report Date
November 8, 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

THE TECH REPLACED THE WORN BRAKE CASTER AND BRAKE/STEER CASTERS TO REPAIR THE STRETCHER.

Description of Event or Problem · 1

INFO RECEIVED INDICATES THE BRAKE WILL NOT HOLD.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 GPS PROCEDURAL STRETCHER AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 881

Patients

Seq Age Sex Outcome Treatment
1