FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 2151349 · Received June 7, 2011

Report

Report Number
1824206-2011-03132
Event Type
Malfunction
Date Received
June 7, 2011
Date of Event
May 16, 2011
Report Date
May 16, 2011
Manufacturer
HILL-ROM INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE TECH ISOLATED THE ISSUE TO THE HEAD DOWN SOLENOID VALVE. HE REPLACED THE SOLENOID VALVE TO REPAIR THE BED.

Description of Event or Problem · 1

INFO RECEIVED INDICATES THE HEAD OF THE BED 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