FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 2421705 · Received January 13, 2012

Report

Report Number
1824206-2012-00241
Event Type
Malfunction
Date Received
January 13, 2012
Date of Event
December 22, 2011
Report Date
December 23, 2011
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

BED IN WAREHOUSE. TECHNICIAN FOUND THE TREND ON THE HYD POWER UNIT WAS LEAKING DUE TO BEING CROSS THREADED. CAUSING UNIT NOT TO GO INTO TRENDELENBURG. REPLACED HYD POWER UNIT TO RESOLVE THIS ISSUE.

Description of Event or Problem · 1

INFORMATION RECEIVED THE BED HAD NO TRENDELENBURG. NO INJURY REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. P1840

Patients

Seq Age Sex Outcome Treatment
1