FDA Adverse Event Malfunction Summary report: N

NON AC-POWERED PATIENT LIFT

MDR report key: 3250934 · Received July 29, 2013

Report

Report Number
3004493922-2013-01647
Event Type
Malfunction
Date Received
July 29, 2013
Report Date
July 10, 2013
Manufacturer
INVACARE SUZHOU
Product Code
FSA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WI, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

THE DEALER ALLEGES THE UNIT IS LEAKING OIL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
353304 NON AC-POWERED PATIENT LIFT 880.5510 FSA INVACARE SUZHOU 9805P

Patients

Seq Age Sex Outcome Treatment
1 Other