FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 2091405 · Received May 5, 2011

Report

Report Number
1824206-2011-02577
Event Type
Malfunction
Date Received
May 5, 2011
Date of Event
April 13, 2011
Report Date
April 13, 2011
Manufacturer
HILL-ROM INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN FOUND THE HEAD UP VALVE WAS STUCK CLOSED. HE REPLACED THE HEAD UP VALVE TO REPAIR THE BED.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATES THE BED HAS NO HEAD UP FUNCTION.

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