FDA Adverse Event Malfunction Summary report: N

REMANUFACTURED BED

MDR report key: 1933242 · Received December 2, 2010

Report

Report Number
1824206-2010-11354
Event Type
Malfunction
Date Received
December 2, 2010
Date of Event
November 8, 2010
Report Date
November 8, 2010
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MD, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN FOUND THE RUBBER TIRES ON THE CASTERS WERE OLD AND CRACKING. THE TECHNICIAN REPLACED THE CASTERS TO REPAIR THE BED.

Description of Event or Problem · 1

DURING A PREVENTIVE MAINTENANCE CHECK, THE TECHNICIAN NOTICED THE CASTERS WERE SLIDING WHEN THE BRAKE WAS ENGAGED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 REMANUFACTURED BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 8400

Patients

Seq Age Sex Outcome Treatment
1