FDA Adverse Event Malfunction Summary report: N

CENTRA BED

MDR report key: 1881594 · Received October 20, 2010

Report

Report Number
1824206-2010-10576
Event Type
Malfunction
Date Received
October 20, 2010
Date of Event
September 24, 2010
Report Date
September 24, 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 TECHNICIAN REPLACED THE BRAKE CASTER TO REPAIR THE BED.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATES THE BRAKE CASTER WOULD LOCK AND HOLD BUT THE CASTER WOULD ROTATE IF PUSHED ON FROM 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