FDA Adverse Event Malfunction Summary report: N

RESIDENT BED

MDR report key: 2220498 · Received July 18, 2011

Report

Report Number
1824206-2011-03792
Event Type
Malfunction
Date Received
July 18, 2011
Date of Event
June 30, 2011
Report Date
June 30, 2011
Manufacturer
HILL-ROM INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MN, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN REPLACED THE CONTROL BOX TO REPAIR THE BED.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATES THE HEAD SECTION IS RAISED TO 45 DEGREES AND WILL NOT GO UP OR DOWN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 RESIDENT BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. 870

Patients

Seq Age Sex Outcome Treatment
1