FDA Adverse Event Malfunction Summary report: N

TOTALCARE BARIATRIC PLUS

MDR report key: 2253093 · Received August 31, 2011

Report

Report Number
1824206-2011-04582
Event Type
Malfunction
Date Received
August 31, 2011
Date of Event
August 6, 2011
Report Date
August 7, 2011
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECH FOUND THE SIDERAIL LATCH PLATE WAS BENT, PREVENTING THE SIDERAIL FROM LATCHING. HE STRAIGHTENED THE LATCH PLATE TO REPAIR THE BED.

Description of Event or Problem · 1

INFO RECEIVED INDICATES THE 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