FDA Adverse Event Malfunction Summary report: N

4 MOTOR ADVANCE BED

MDR report key: 1920929 · Received December 6, 2010

Report

Report Number
1824206-2010-11404
Event Type
Malfunction
Date Received
December 6, 2010
Date of Event
November 10, 2010
Report Date
November 10, 2010
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE ACCOUNT MANUALLY CRANKED DOWN THE HEAD SECTION AND ISOLATED THE SIDERAILS. THE ACCOUNT FOUND WITH THE LEFT SIDERAIL UNPLUGGED THE HEAD SECTION DOES NOT RISE. THE ACCOUNT REPLACED THE LEFT SIDERAIL SWITCH PACKAGE TO REPAIR THE BED.

Description of Event or Problem · 1

THE ACCOUNT ALLEGED THE HEAD SECTION ROSE ON ITS OWN WHEN THE BED WAS PLUGGED IN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 4 MOTOR ADVANCE BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1115

Patients

Seq Age Sex Outcome Treatment
1