FDA Adverse Event Malfunction Summary report: N

4 MOTOR ADVANCE BED

MDR report key: 1191427 · Received September 25, 2008

Report

Report Number
1824206-2008-03461
Event Type
Malfunction
Date Received
September 25, 2008
Date of Event
August 27, 2008
Report Date
August 27, 2008
Manufacturer
HILL-ROM RITTER
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MO, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

THE HILL-ROM FIELD TECHNICIAN REPORTED THAT THIS BED HAD AN UNINTENTIONAL DOWNWARD MOVEMENT. HE FOUND THAT ONE OF THE CONTROL CABLES WAS SHORTED INTERNALLY. REPLACEMENT OF THE CABLE RESOLVED THE ISSUE. THERE WERE NO REPORTED ADVERSE EVENTS ASSOCIATED WITH THIS PRODUCT PROBLEM.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 4 MOTOR ADVANCE BED AC POWERED HOSPITAL BED FNL HILL-ROM RITTER 1105 NA

Patients

Seq Age Sex Outcome Treatment
1