FDA Adverse Event Malfunction Summary report: N

CENTRA BED

MDR report key: 1821780 · Received August 26, 2010

Report

Report Number
1824206-2010-09595
Event Type
Malfunction
Date Received
August 26, 2010
Date of Event
August 3, 2010
Report Date
August 3, 2010
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 TECH REPLACED THE BRAKE CASTER TO REPAIR THE BED.

Description of Event or Problem · 1

INFO RECEIVED INDICATES THE BRAKE WOULD LOCK AND HOLD, BUT THE CASTER WOULD CONTINUE TO ROTATE IF PUSHED ON THE SIDE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CENTRA BED AC POWERED HOSPITAL BED FNL HILL-ROM, INC. 850

Patients

Seq Age Sex Outcome Treatment
1