FDA Adverse Event Malfunction Summary report: N

TOTALCARE BARIATRIC

MDR report key: 1882719 · Received October 21, 2010

Report

Report Number
1824206-2010-10589
Event Type
Malfunction
Date Received
October 21, 2010
Date of Event
September 27, 2010
Report Date
September 27, 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 OBSERVED THE BED FOR A COUPLE OF DAYS AND COULD NOT DUPLICATE THE ALLEGED MALFUNCTION.

Description of Event or Problem · 1

INFO RECEIVED INDICATES THE NURSE PLUGGED THE BED IN AND THE BED STARTED SMOKING. A PATIENT WAS NOT IN THE BED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE BARIATRIC AC POWERED HOSPITAL BED FNL HILL-ROM INC 1840

Patients

Seq Age Sex Outcome Treatment
1