FDA Adverse Event Malfunction Summary report: N

TOTALCARE BARIATRIC

MDR report key: 1891377 · Received November 2, 2010

Report

Report Number
1824206-2010-10800
Event Type
Malfunction
Date Received
November 2, 2010
Date of Event
October 7, 2010
Report Date
October 7, 2010
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
DC, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE TECH FOUND THE LATCH COVER PLATE WAS HOOKED ON THE LATCH HOOK ON THE INSIDE OF THE SIDERAIL ARM. THE TECH ADJUSTED THE LATCH COVER TO THE CORRECT POSITION TO REPAIR THE BED.

Description of Event or Problem · 1

INFO RECEIVED INDICATES THE LEFT HEAD SIDERAIL IS NOT LATCHING.

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