FDA Adverse Event Malfunction Summary report: N

TOTALCARE BARIATRIC

MDR report key: 1934271 · Received December 3, 2010

Report

Report Number
1824206-2010-11382
Event Type
Malfunction
Date Received
December 3, 2010
Date of Event
November 9, 2010
Report Date
November 16, 2010
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WV, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECH REMOVED THE HEAD UP VALVE, CLEANED AND REINSTALLED THE VALVE TO REPAIR THE BED.

Description of Event or Problem · 1

INFO RECEIVED INDICATES THE HEAD OF THE BED WILL NOT RISE.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1