FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 1960121 · Received December 17, 2010

Report

Report Number
1824206-2010-11764
Event Type
Malfunction
Date Received
December 17, 2010
Date of Event
November 23, 2010
Report Date
November 23, 2010
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE ACCOUNT HAS NOT RETURNED HILL-ROM'S ATTEMPTS TO DETERMINE THE RESOLUTION OF THE ALLEGED MALFUNCTION.

Description of Event or Problem · 1

THE ACCOUNT ALLEGED THE FOOT HI/LOW FUNCTION IS DRIFTING DOWN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1900

Patients

Seq Age Sex Outcome Treatment
1