FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 2760331 · Received September 20, 2012

Report

Report Number
1824206-2012-05668
Event Type
Malfunction
Date Received
September 20, 2012
Date of Event
August 28, 2012
Report Date
August 28, 2012
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECH ISOLATED THE ISSUE TO THE HEAD UP VALVE. HE REPLACED THE HEAD UP VALVE AND THE BED FUNCTIONED PROPERLY.

Description of Event or Problem · 1

INFO RECEIVED INDICATES THE HEAD UP FUNCTION IS NOT WORKING MANUALLY OR UNDER POWER.

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