FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 2033137 · Received February 28, 2011

Report

Report Number
1824206-2011-01157
Event Type
Malfunction
Date Received
February 28, 2011
Date of Event
February 3, 2011
Report Date
February 3, 2011
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

AFTER REPLACING THE HEAD UP AND DOWN VALVES, THE ACCOUNTS MAINTENANCE REPLACED THE HYDRAULIC MANIFOLD TO REPAIR THE BED.

Description of Event or Problem · 1

INFO RECEIVED INDICATES THE HEAD UP FUNCTION IS NOT WORKING ON THE BED.

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