FDA Adverse Event Malfunction Summary report: N

TOTALCARE BARIATRIC PLUS BED

MDR report key: 2942238 · Received January 4, 2013

Report

Report Number
1824206-2013-00109
Event Type
Malfunction
Date Received
January 4, 2013
Date of Event
May 24, 2011
Report Date
December 18, 2012
Manufacturer
HILL-ROM INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN REPLACED THE TRENDELENBERG VALVE TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

THE TECHNICIAN ALLEGED THAT THE BED HAD NO TRENDELENBURG FUNCTION. NO PT IMPACT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
4884 TOTALCARE BARIATRIC PLUS BED AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. 1840

Patients

Seq Age Sex Outcome Treatment
1