FDA Adverse Event Malfunction Summary report: N

4 MOTOR ADVANCE BED

MDR report key: 2233350 · Received July 20, 2011

Report

Report Number
1824206-2011-03843
Event Type
Malfunction
Date Received
July 20, 2011
Date of Event
July 6, 2011
Report Date
July 6, 2011
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE ACCOUNT REPLACED THE COMPLETE LEFT HEAD SIDERAIL TO REPAIR THE BED.

Description of Event or Problem · 1

THE ACCOUNTS MAINTENANCE STATED THE HEAD SECTION RISES UNINTENTIONALLY WHEN HE TURNS THE LOCKOUTS OFF AT THE FOOTBOARD. WHEN THE LEFT SIDERAIL IS UNPLUGGED THE HEAD SECTION DOESN'T RAISE UNINTENTIONALLY.

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. 1165

Patients

Seq Age Sex Outcome Treatment
1