FDA Adverse Event Malfunction Summary report: N

CENTRA BED

MDR report key: 2024048 · Received March 11, 2011

Report

Report Number
1824206-2011-01471
Event Type
Malfunction
Date Received
March 11, 2011
Date of Event
February 15, 2011
Report Date
February 15, 2011
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN INSPECTED THE BRAKE CASTERS AND FOUND THE RIGHT HEAD BRAKE CASTER WHEEL LOCKS BUT PIVOTS IN A CIRCLE. HE REPLACED THE RIGHT HEAD BRAKE CASTER TO REPAIR THE BED.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATES THE BED WILL NOT BRAKE PROPERLY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CENTRA BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1062

Patients

Seq Age Sex Outcome Treatment
1