FDA Adverse Event Malfunction Summary report: N

4 MOTOR ADVANCE BED

MDR report key: 1205109 · Received October 8, 2008

Report

Report Number
1824206-2008-03731
Event Type
Malfunction
Date Received
October 8, 2008
Date of Event
September 15, 2008
Report Date
September 15, 2008
Manufacturer
HILL-ROM RITTER
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE FACILITIES MAINTENANCE INDICATED THE HEAD SECTION OF THE BED WOULD MOVE UP UNINTENTIONALLY. THE FACILITIES MAINTENANCE FOUND FLUID INGRESS IN THE SIDERAIL BOARD. THE SIDERAIL BOARD WAS CLEANED, AND DRIED TO REPAIR THE BED.

Description of Event or Problem · 1

INFO RECEIVED INDICATES UNINTENTIONAL MOVEMENT OF THE HEAD SECTION FUNCTION UP.

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

Patients

Seq Age Sex Outcome Treatment
1 UNK