FDA Adverse Event Malfunction Summary report: N

TOTALCARE BARIATRIC PLUS

MDR report key: 2863112 · Received November 1, 2012

Report

Report Number
1824206-2012-07043
Event Type
Malfunction
Date Received
November 1, 2012
Date of Event
January 25, 2011
Report Date
January 25, 2011
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IN, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN REPLACED THE LATCH COVER, AND THE SIDERAIL IS NOT FUNCTIONING PROPERLY.

Description of Event or Problem · 1

INFO RECEIVED INDICATES WHILE PERFORMING AN INSPECTION OF THE BED, THE TECHNICIAN FOUND THE RIGHT INTERMEDIATE SIDERAIL LATCH COVER BENT, WHICH PREVENTED THE SIDERAIL FROM LOCKING IN PLACE.

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