FDA Adverse Event Malfunction Summary report: N

TOTALCARE BARIATRIC PLUS BED

MDR report key: 2902943 · Received November 29, 2012

Report

Report Number
1824206-2012-07783
Event Type
Malfunction
Date Received
November 29, 2012
Date of Event
November 7, 2012
Report Date
November 7, 2012
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN REPLACED THE HEAD UP VALVE TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

THE TECHNICIAN ALLEGED THAT THE HEAD OF THE BED WILL NOT RAISE. NO PATIENT 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