FDA Adverse Event Malfunction Summary report: N

TOTALCARE BARIATRIC PLUS BED

MDR report key: 2922688 · Received December 27, 2012

Report

Report Number
1824206-2012-08653
Event Type
Malfunction
Date Received
December 27, 2012
Date of Event
December 10, 2012
Report Date
December 10, 2012
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CO, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE TECH REPLACED THE HEAD UP HYDRAULIC VALVE TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

THE ACCOUNT ALLEGED THAT THE BED HAS NO HEAD UP FUNCTION. NO PT IMPACT.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1