FDA Adverse Event Malfunction Summary report: N

TOTALCARE BARIATRIC PLUS

MDR report key: 2863147 · Received November 1, 2012

Report

Report Number
1824206-2012-07047
Event Type
Malfunction
Date Received
November 1, 2012
Date of Event
January 27, 2011
Report Date
January 27, 2011
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AZ, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN LUBRICATED THE SIDERAIL LATCH MECHANISM AND THE SIDERAIL IS NOT FUNCTIONING PROPERLY.

Description of Event or Problem · 1

INFO RECEIVED INDICATES THE LEFT FOOT SIDERAIL WILL NOT LATCH.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1