FDA Adverse Event Malfunction Summary report: N

TOTALCARE BARIATRIC

MDR report key: 2901941 · Received November 21, 2012

Report

Report Number
1824206-2012-07659
Event Type
Malfunction
Date Received
November 21, 2012
Date of Event
November 1, 2012
Report Date
November 1, 2012
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IN, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATED THAT THE LEFT INTERMEDIATE SIDERAIL WOULD 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