FDA Adverse Event Malfunction Summary report: N

3 MOTOR ADVANCE BED

MDR report key: 2172073 · Received June 21, 2011

Report

Report Number
1824206-2011-03345
Event Type
Malfunction
Date Received
June 21, 2011
Date of Event
April 28, 2011
Report Date
April 28, 2011
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TN, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE ACCOUNT HAS NOT RETURNED HILL-ROM'S ATTEMPTS TO DETERMINE THE RESOLUTION OF THE ALLEGED MALFUNCTION.

Description of Event or Problem · 1

INFO RECEIVED INDICATES THE SIDERAIL WELDS ARE BROKEN WHICH IS PREVENTING THE SIDERAIL FROM LATCHING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 3 MOTOR ADVANCE BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1130

Patients

Seq Age Sex Outcome Treatment
1