FDA Adverse Event Malfunction Summary report: N

CENTRA BED

MDR report key: 1960126 · Received December 17, 2010

Report

Report Number
1824206-2010-11701
Event Type
Malfunction
Date Received
December 17, 2010
Date of Event
November 29, 2010
Report Date
November 29, 2010
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

TECH CLEANED AND DEGREASED THE HI/LOW BRAKE TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

TECH ALLEGED THAT THE BED WILL NOT STAY UP. THE BED WOULD LOWER VERY SLOWLY WHEN RAISED UP. 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