FDA Adverse Event Malfunction Summary report: N

TOTALCARE BARIATRIC PLUS BED

MDR report key: 2974638 · Received January 29, 2013

Report

Report Number
1824206-2013-00746
Event Type
Malfunction
Date Received
January 29, 2013
Date of Event
January 16, 2013
Report Date
January 16, 2013
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

NO FURTHER INFO IS AVAILABLE ON THE REPAIR OF THE BED AT THIS TIME.

Description of Event or Problem · 1

THE ACCOUNT ALLEGED THE BED HAD NO FUNCTIONS ELECTRICALLY OR MANUALLY. NO PT IMPACT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
39784 TOTALCARE BARIATRIC PLUS BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1840

Patients

Seq Age Sex Outcome Treatment
1