FDA Adverse Event Malfunction Summary report: N

TOTALCARE BED

MDR report key: 2942335 · Received January 8, 2013

Report

Report Number
1824206-2013-00192
Event Type
Malfunction
Date Received
January 8, 2013
Date of Event
December 21, 2012
Report Date
December 21, 2012
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

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

Description of Event or Problem · 1

INFO RECEIVED INDICATED THE HEAD SECTION WOULD NOT RAISE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
9885 TOTALCARE BED AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1900

Patients

Seq Age Sex Outcome Treatment
1