FDA Adverse Event Malfunction Summary report: N

GPS PROCEDURAL STRETCHER

MDR report key: 2233292 · Received July 22, 2011

Report

Report Number
1824206-2011-03899
Event Type
Malfunction
Date Received
July 22, 2011
Date of Event
July 11, 2011
Report Date
July 11, 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 ADJUSTED THE BRAKE TO REPAIR THE BED.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATES THE FOOT BRAKE CASTER IS NOT WORKING OR HOLDING PROPERLY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 GPS PROCEDURAL STRETCHER WHEELED STRETCHER FPO HILL-ROM INC. 881

Patients

Seq Age Sex Outcome Treatment
1