FDA Adverse Event Malfunction Summary report: N

TOTALCARE BARIATRIC

MDR report key: 1851986 · Received September 24, 2010

Report

Report Number
1824206-2010-10101
Event Type
Malfunction
Date Received
September 24, 2010
Date of Event
August 27, 2010
Report Date
August 27, 2010
Manufacturer
HILL-ROM INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

TECHNICIAN FOUND THE HYDRAULIC VALVE SOLENOID IS STUCK. TECHNICIAN REPLACED THE VALVE AND THE BED IS WORKING FINE NOW.

Description of Event or Problem · 1

ACCOUNT ALLEGED THAT THE HEAD OF THE BED WOULD NOT GO UP. NO INJURY REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE BARIATRIC A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. P1840

Patients

Seq Age Sex Outcome Treatment
1