FDA Adverse Event Malfunction Summary report: N

NON AC-POWERED PATIENT LIFT

MDR report key: 3200403 · Received July 1, 2013

Report

Report Number
3004493922-2013-01373
Event Type
Malfunction
Date Received
July 1, 2013
Report Date
June 5, 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 PROVIDER REPORTED THE THE HANDLE ON THE 9099P HYDRAULIC PUMP HAS BROKEN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
299034 NON AC-POWERED PATIENT LIFT 880.5510 FSA INVACARE SUZHOU 9099P

Patients

Seq Age Sex Outcome Treatment
1 Other