FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 1990060 · Received January 28, 2011

Report

Report Number
1824206-2011-00511
Event Type
Malfunction
Date Received
January 28, 2011
Date of Event
January 6, 2011
Report Date
January 6, 2011
Manufacturer
HILL-ROM INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IN, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

TECHNICIAN FOUND THAT MULTIPLE HYDRAULIC FUNCTIONS WERE NOT OPERATING ON THIS BED. ISOLATED THE PROBLEM TO HYDRAULIC MANIFOLD. REPLACED HYDRAULIC MANIFOLD TO RESOLVE THIS ISSUE.

Description of Event or Problem · 1

ALLEGATION RECEIVED THAT MULTIPLE HYDRAULIC FUNCTIONS WERE NOT OPERATING ON THIS BED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. P1900F005566

Patients

Seq Age Sex Outcome Treatment
1