FDA Adverse Event Malfunction Summary report: N

CCU

MDR report key: 2233284 · Received July 22, 2011

Report

Report Number
1824206-2011-03891
Event Type
Malfunction
Date Received
July 22, 2011
Date of Event
July 6, 2011
Report Date
July 6, 2011
Manufacturer
HILL-ROM INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN REPLACE THE CASTERS TO REPAIR THE BED.

Description of Event or Problem · 1

INFO REC'D INDICATES THE BRAKE CASTER AT THE FOOT END OF THE BED WILL LOCK IN PLACE AND NOT ROLL BUT WOULD CONTINUE TO SWIVEL. THE CASTER COULD NOT BE ADJUSTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CCU AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. 894

Patients

Seq Age Sex Outcome Treatment
1