FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 1934292 · Received December 3, 2010

Report

Report Number
1824206-2010-11388
Event Type
Malfunction
Date Received
December 3, 2010
Date of Event
November 9, 2010
Report Date
November 9, 2010
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 REPLACED THE HEAD VALVE GUIDE TUBE TO REPAIR THE BED.

Description of Event or Problem · 1

INFO REC'D INDICATES THE HEAD UP IS NOT WORKING WHEN DEPRESSING THE HEAD UP BUTTON OPTION. THE FUNCTION WILL ALSO NOT WORK MANUALLY.

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