FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 2000079 · Received February 3, 2011

Report

Report Number
1824206-2011-00639
Event Type
Malfunction
Date Received
February 3, 2011
Date of Event
January 12, 2011
Report Date
January 12, 2011
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

TECHNICIAN INSPECTED THE HYD SYSTEM AND FOUND THE FOOT PILOT CHECK VALVE WAS BAD. REPLACED THE PILOT FOOT CHECK VALVE TO RESOLVE THIS ISSUE.

Description of Event or Problem · 1

COMPLAINT ALLEGED THAT THE FOOT SECTION OF SLEEP DECK WOULD DRIFT DOWN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. P1900H006263

Patients

Seq Age Sex Outcome Treatment
1