FDA Adverse Event Malfunction Summary report: N

TOTALCARE BARIATRIC

MDR report key: 1993558 · Received January 24, 2011

Report

Report Number
1824206-2011-00429
Event Type
Malfunction
Date Received
January 24, 2011
Date of Event
December 28, 2010
Report Date
December 28, 2010
Manufacturer
HILL-ROM INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MD, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN FOUND THE SIDERAIL ARM ASSEMBLY WAS CRACKED. HE REPLACED THE SIDERAIL ARM TO REPAIR THE BED.

Description of Event or Problem · 1

INFO RECEIVED INDICATES THE HEAD SIDERAIL WILL NOT LATCH.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1