FDA Adverse Event Malfunction Summary report: N

NON AC-POWERED PATIENT LIFT

MDR report key: 3191823 · Received June 26, 2013

Report

Report Number
3004493922-2013-01340
Event Type
Malfunction
Date Received
June 26, 2013
Report Date
May 31, 2013
Manufacturer
INVACARE SUZHOU
Product Code
FSA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

THE END USER STATED THE HYDRAULIC LIFT WILL NO LONGER STAY UP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
290497 NON AC-POWERED PATIENT LIFT 880.5510 FSA INVACARE SUZHOU 9805

Patients

Seq Age Sex Outcome Treatment
1 Other