FDA Adverse Event Malfunction Summary report: N

TOTAL CARE

MDR report key: 2053612 · Received March 17, 2011

Report

Report Number
1824206-2011-01658
Event Type
Malfunction
Date Received
March 17, 2011
Date of Event
February 25, 2011
Report Date
February 25, 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

TECHNICIAN FOUND THAT THE FOOT HI/LOW WOULD DRIFTS DOWN. REPLACED HYDRAULIC MANIFOLD TO RESOLVE THIS ISSUE. BED FOUND IN ICU.

Description of Event or Problem · 1

COMPLAINT ALLEGED THAT THE FOOT HI/LOW DRIFTS DOWN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTAL CARE AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. P1830ACAP

Patients

Seq Age Sex Outcome Treatment
1