FDA Adverse Event Malfunction Summary report: N

REMANUFACTURED BED

MDR report key: 2151441 · Received June 8, 2011

Report

Report Number
1824206-2011-03163
Event Type
Malfunction
Date Received
June 8, 2011
Date of Event
May 18, 2011
Report Date
May 18, 2011
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

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

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATES THE BED'S HEAD SECTION BRAKE IS NOT HOLDING. FOOT END BRAKE IS WORKING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 REMANUFACTURED BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 8200

Patients

Seq Age Sex Outcome Treatment
1