FDA Adverse Event Malfunction Summary report: N

CENTRA BED

MDR report key: 1993232 · Received January 21, 2011

Report

Report Number
1824206-2011-00422
Event Type
Malfunction
Date Received
January 21, 2011
Date of Event
December 30, 2010
Report Date
December 30, 2010
Manufacturer
HILL-ROM INC
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN ADJUSTED THE REVERSE TREND MICRO SWITCH TO REPAIR THE BED.

Description of Event or Problem · 1

INFO REC'D INDICATES, THE BED WILL NOT GO INTO REVERSE TRENDELENBURG.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1