FDA Adverse Event Malfunction Summary report: N

TOTALCARE BED

MDR report key: 1905689 · Received November 12, 2010

Report

Report Number
1824206-2010-10995
Event Type
Malfunction
Date Received
November 12, 2010
Date of Event
October 19, 2010
Report Date
October 19, 2010
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OK, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN REPLACED THE HYDRAULIC SOLENOID VALVE TO REPAIR THE BED.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATES THE HEAD OF THE BED CANNOT BE RAISED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1900

Patients

Seq Age Sex Outcome Treatment
1