FDA Adverse Event Malfunction Summary report: N

3 MOTOR ADVANCE BED

MDR report key: 1811378 · Received August 17, 2010

Report

Report Number
1824206-2010-09374
Event Type
Malfunction
Date Received
August 17, 2010
Date of Event
July 23, 2010
Report Date
July 23, 2010
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
LA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN ATTEMPTED TO ADJUST THE BRAKE, BUT IT DID NOT RESOLVE THE ISSUE. THE TECHNICIAN FOUND THE BED HAD THE OLD STYLE CENTER BLOCK BEARINGS. HE REPLACED THE BEARINGS AND STIFFENER PLATE TO REPAIR THE BED.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATES WHEN THE BRAKES ARE ACTIVATED, THE BRAKE/STEER CASTER AND THE BRAKE CASTER WOULD NOT ROLL, BUT WOULD RATCHET FROM SIDE TO SIDE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 3 MOTOR ADVANCE BED AC POWERED HOSPITAL BED FNL HILL-ROM, INC. 1130

Patients

Seq Age Sex Outcome Treatment
1