FDA Adverse Event Malfunction Summary report: N

CENTRA BED

MDR report key: 1952420 · Received January 3, 2011

Report

Report Number
1824206-2011-00021
Event Type
Malfunction
Date Received
January 3, 2011
Date of Event
December 13, 2010
Report Date
December 13, 2010
Manufacturer
HILL-ROM INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

TECHNICIAN FOUND THE FLOATING BRAKE IS WORN AND GREASY. TECHNICIAN REPLACED THE FLOATING BRAKE DRUM TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

TECHNICIAN ALLEGED THAT THE HI/LOW IS DRIFTING DOWN AFTER IT IS LOWERED AND HAS INTERMITTENT NOISE. NO PT IMPACT.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1