FDA Adverse Event Malfunction Summary report: N

TOTALCARE BARIATRIC

MDR report key: 3031348 · Received March 5, 2013

Report

Report Number
1824206-2013-01242
Event Type
Malfunction
Date Received
March 5, 2013
Date of Event
February 6, 2013
Report Date
February 6, 2013
Manufacturer
HILL-ROM INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CO, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE HILL-ROM TECHNICIAN REPLACED THE HEAD HI-LO VALVE TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATED THE HEAD HI-LO DRIFTS DOWN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
94888 TOTALCARE BARIATRIC AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. 1840

Patients

Seq Age Sex Outcome Treatment
1