FDA Adverse Event Malfunction Summary report: N

TOTALCARE BARIATRIC PLUS BED

MDR report key: 2942273 · Received January 4, 2013

Report

Report Number
1824206-2013-00123
Event Type
Malfunction
Date Received
January 4, 2013
Date of Event
December 18, 2012
Report Date
December 18, 2012
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SC, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN FOUND THE GROUND PRONG BROKEN INSIDE THE MOLDED END OF THE POWER CORD. THE TECHNICIAN REPLACED THE POWER CORD TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

THE TECHNICIAN ALLEGED THAT THE BED DID NOT PASS THE GROUND RESISTANCE TEST. NO PATIENT IMPACT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
5788 TOTALCARE BARIATRIC PLUS BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1840

Patients

Seq Age Sex Outcome Treatment
1