FDA Adverse Event Malfunction Summary report: N

TOTALCARE BED

MDR report key: 2974702 · Received January 18, 2013

Report

Report Number
1824206-2013-00547
Event Type
Malfunction
Date Received
January 18, 2013
Date of Event
January 9, 2013
Report Date
January 9, 2013
Manufacturer
HILL-ROM INC
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN REPLACED THE HEAD UP VALVE TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

THE TECHNICIAN ALLEGED THE BED HAD NO HEAD UP FUNCTION. NO PT IMPACT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
28656 TOTALCARE BED AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC 1900

Patients

Seq Age Sex Outcome Treatment
1