FDA Adverse Event Malfunction Summary report: N

NON AC-POWERED PATIENT LIFT

MDR report key: 3024236 · Received March 27, 2013

Report

Report Number
3004493922-2013-00686
Event Type
Malfunction
Date Received
March 27, 2013
Report Date
February 28, 2013
Manufacturer
INVACARE SUZHOU
Product Code
FSA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PROVIDER/TBM STATE THE PUMP IS LEAKING AND LIFT WILL NOT GO DOWN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
126558 NON AC-POWERED PATIENT LIFT 880.5510 FSA INVACARE SUZHOU 9805P

Patients

Seq Age Sex Outcome Treatment
1 Other