FDA Adverse Event Malfunction Summary report: N

TOTALCARE BARIATRIC

MDR report key: 1853762 · Received September 29, 2010

Report

Report Number
1824206-2010-10193
Event Type
Malfunction
Date Received
September 29, 2010
Date of Event
September 3, 2010
Report Date
September 3, 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 FOUND THE BED SHROUD COVER WAS OUT OF PLACE ALLOWING THE CPR LEVER TO ENGAGE WHILE BEING WEDGED UNDER THE COVER. THE TECHNICIAN PROPERLY POSITIONED THE COVER TO REPAIR THE BED.

Description of Event or Problem · 1

THE ACCOUNT ALLEGED NO BED FUNCTIONS ARE WORKING.

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