FDA Adverse Event Malfunction Summary report: N

NON AC-POWERED PATIENT LIFT

MDR report key: 3163569 · Received June 11, 2013

Report

Report Number
3004493922-2013-01253
Event Type
Malfunction
Date Received
June 11, 2013
Report Date
May 15, 2013
Manufacturer
INVACARE SUZHOU
Product Code
FSA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PROVIDER STATED NORMAL OIL LEAK. RELEASE LEVER LOOSE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
263986 NON AC-POWERED PATIENT LIFT 880.5510 FSA INVACARE SUZHOU 9805

Patients

Seq Age Sex Outcome Treatment
1 Other