FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 1132424 · Received August 22, 2008

Report

Report Number
1824206-2008-03177
Event Type
Malfunction
Date Received
August 22, 2008
Date of Event
August 12, 2008
Report Date
August 12, 2008
Manufacturer
HILL-ROM RITTER
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

REP ALLEGED THE HI/LOW UP HAD UNINTENTIONAL MOVEMENT. NO INJURY REPORTED. UNIT MOVING ERRATICALLY CAUSE - U.C.M. DAMAGED BY FLUID BUILD UP, RESOLVE - REPLACED U.C.M.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE AC POWERED HOSPITAL BED FNL HILL-ROM RITTER 1900 P1900F005565

Patients

Seq Age Sex Outcome Treatment
1