FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 1112733 · Received August 11, 2008

Report

Report Number
1824206-2008-03032
Event Type
Malfunction
Date Received
August 11, 2008
Date of Event
July 9, 2008
Report Date
July 9, 2008
Manufacturer
HILL-ROM RITTER
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OR, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

IN 2008, REP STATED THE BED HAS NO FUNCTIONS. HE SAID NOBODY WAS HURT. TWO DAYS LATER, REP CALLED IN STATING BED IS BACK IN SERVICE. HE REPLACED THE F1 FUSE AND THIS TOOK CARE OF PROBLEM.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE AC POWERED HOSPITAL BED FNL HILL-ROM RITTER 1900 P1900D004731

Patients

Seq Age Sex Outcome Treatment
1