FDA Adverse Event Malfunction Summary report: N

CENTRA BED

MDR report key: 2020097 · Received March 10, 2011

Report

Report Number
1824206-2011-01440
Event Type
Malfunction
Date Received
March 10, 2011
Date of Event
February 13, 2011
Report Date
February 13, 2011
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN REPLACED THE BRAKE BUSHINGS AND CASTERS TO REPAIR THE BED.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATES, THE BED HAS NO BRAKE AFTER SETTING THE BRAKE PEDAL INTO THE BRAKE POSITION. THE BED WOULD ROLL AND STAY IN STEER.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1