FDA Adverse Event Malfunction Summary report: N

TOTALCARE BARIATRIC

MDR report key: 1883914 · Received October 22, 2010

Report

Report Number
1824206-2010-10628
Event Type
Malfunction
Date Received
October 22, 2010
Date of Event
September 28, 2010
Report Date
September 28, 2010
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 TECHNICIAN RECALIBRATED THE HEAD HI/LOW LIMITS TO REPAIR THE BED.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATES THE HEAD SECTION WILL NOT GO UP OR DOWN AND THE BED WILL NOT GO INTO THE CHAIR POSITION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE BARIATRIC AC POWERED HOSPITAL BED FNL HILL-ROM, INC. 1840

Patients

Seq Age Sex Outcome Treatment
1