FDA Adverse Event Malfunction Summary report: N

TOTALCARE BARIATRIC PLUS

MDR report key: 2922676 · Received December 27, 2012

Report

Report Number
1824206-2012-08659
Event Type
Malfunction
Date Received
December 27, 2012
Date of Event
December 13, 2012
Report Date
December 13, 2012
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE TECH INSPECTED THE BED AND COULD NOT DUPLICATE THE ALLEGED MALFUNCTION. ALL BED FUNCTIONS WERE WORKING CORRECTLY.

Description of Event or Problem · 1

INFO RECEIVED INDICATES THE HEAD OF THE BED CANNOT BE RAISED.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1 UNK