FDA Adverse Event Malfunction Summary report: N

NON AC-POWERED PATIENT LIFT

MDR report key: 3180984 · Received June 20, 2013

Report

Report Number
3004493922-2013-01309
Event Type
Malfunction
Date Received
June 20, 2013
Report Date
May 28, 2013
Manufacturer
INVACARE SUZHOU
Product Code
FSA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MN, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PROVIDER STATES LEAKING GREASE OR OIL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
279851 NON AC-POWERED PATIENT LIFT 880.5510 FSA INVACARE SUZHOU GHS350

Patients

Seq Age Sex Outcome Treatment
1 Other