FDA Adverse Event Malfunction Summary report: N

4 MOTOR ADVANCE BED

MDR report key: 2100197 · Received May 16, 2011

Report

Report Number
1824206-2011-02705
Event Type
Malfunction
Date Received
May 16, 2011
Date of Event
April 21, 2011
Report Date
April 21, 2011
Manufacturer
HILL-ROM INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE BIOMED COULD NOT DUPLICATE THE ALLEGED MALFUNCTION. HE IS GOING TO ISOLATE THE SIDERAILS AND TEST PORT. HIS INVESTIGATION HAS NOT BEEN COMPLETED.

Description of Event or Problem · 1

INFO RECEIVED INDICATES THE HEAD SECTION IS DRIFTING DOWN ON ITS OWN.

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. 1145

Patients

Seq Age Sex Outcome Treatment
1