FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 1812834 · Received August 12, 2010

Report

Report Number
1824206-2010-09295
Event Type
Malfunction
Date Received
August 12, 2010
Date of Event
July 20, 2010
Report Date
July 20, 2010
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN FOUND THE HEAD CYLINDER WAS LEAKING. THE TECHNICIAN REPLACED THE CYLINDER AND CALIBRATED THE POSITION SENSORS TO REPAIR THE BED.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATES THE HEAD WILL NOT RISE NOR WILL THE BED GO INTO THE CHAIR POSITION.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1