FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 2072777 · Received March 31, 2011

Report

Report Number
1824206-2011-01955
Event Type
Malfunction
Date Received
March 31, 2011
Date of Event
March 10, 2011
Report Date
March 10, 2011
Manufacturer
HILL-ROM INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

TECHNICIAN FOUND THAT THE HEAD OF THE BED COULD NOT BE RAISED. REPLACED BOTH SIDERAIL UCM PCBS BECAUSE THE HEAD DOWN BUTTONS WERE NOT WORKING ON EITHER SIDERAIL TO RESOLVE THIS ISSUE.

Description of Event or Problem · 1

INFO RECEIVED INDICATED THAT THE HEAD DOWN BUTTONS WERE NOT WORKING ON EITHER SIDERAIL. NO PT IMPACT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. P1900

Patients

Seq Age Sex Outcome Treatment
1