FDA Adverse Event Malfunction Summary report: N

CCU BED

MDR report key: 2233285 · Received July 22, 2011

Report

Report Number
1824206-2011-03896
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
CO, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN FOUND THE CASTER WAS WORN. HE REPLACED THE LEFT HEAD CASTER TO REPAIR THE BED.

Description of Event or Problem · 1

INFO REC'D INDICATES THE CASTER WILL LOCK AND HOLD IN BRAKE BUT CONTINUES TO ROTATE IF PUSHED.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1