FDA Adverse Event Malfunction Summary report: N

TOTALCARE BARIATRIC

MDR report key: 2140347 · Received June 16, 2011

Report

Report Number
1824206-2011-03281
Event Type
Malfunction
Date Received
June 16, 2011
Date of Event
May 23, 2011
Report Date
May 24, 2011
Manufacturer
HILL-ROM INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CO, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECH FOUND THE MOLEX CONNECTION ON THE LEFT SIDERAIL WOULD NOT STAY CONNECTED. HE REPLACED THE SIDERAIL CIRCUIT BOARD TO REPAIR THE BED.

Description of Event or Problem · 1

INFO RECEIVED INDICATES THE BED HAS NO ARTICULATION FUNCTIONS.

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