FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 1881456 · Received October 19, 2010

Report

Report Number
1824206-2010-10556
Event Type
Malfunction
Date Received
October 19, 2010
Date of Event
September 23, 2010
Report Date
September 23, 2010
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN REPLACED THE POWER CONTROL MODULE AND RE-CALIBRATED POSITION SENSORS TO REPAIR THE BED.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATES THE BED CONTROLS ARE NOT WORKING. THE BED HAS NO MANUAL OR ELECTRICAL FUNCTIONS BUT IT DOES HAVE POWER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE AC POWERED HOSPITAL BED FNL HILL-ROM, INC. 1900

Patients

Seq Age Sex Outcome Treatment
1