FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 1813204 · Received August 18, 2010

Report

Report Number
1824206-2010-09407
Event Type
Malfunction
Date Received
August 18, 2010
Date of Event
July 25, 2010
Report Date
July 25, 2010
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN FOUND THE F5 FUSE BLOWN ON THE POWER CONTROL MODULE. THE TECHNICIAN REPLACED THE FUSE TO REPAIR THE BED.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATES THE BED HAS NO 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