FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 2233266 · Received July 22, 2011

Report

Report Number
1824206-2011-03880
Event Type
Malfunction
Date Received
July 22, 2011
Date of Event
July 6, 2011
Report Date
July 7, 2011
Manufacturer
HILL-ROM INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OR, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

TECHNICIAN FOUND THE BED HAD SLOW HEAD DOWN DRIFT. REPLACED THE HEAD DOWN SOLENOID VALVE TO RESOLVE THIS ISSUE.

Description of Event or Problem · 1

INFO PROVIDED INDICATED THAT THE BED HAD A SLOW DRIFT DOWN. NO INJURY ALLEGED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. P1900

Patients

Seq Age Sex Outcome Treatment
1