FDA Adverse Event Malfunction Summary report: N

NON AC-POWERED PATIENT LIFT

MDR report key: 3243278 · Received July 23, 2013

Report

Report Number
3004493922-2013-01594
Event Type
Malfunction
Date Received
July 23, 2013
Report Date
July 2, 2013
Manufacturer
INVACARE SUZHOU
Product Code
FSA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CT, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER ADVISED PUMP DOES NOT HOLD AND GREASE CAME OUT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
342749 NON AC-POWERED PATIENT LIFT 880.5510 FSA INVACARE SUZHOU GHS350

Patients

Seq Age Sex Outcome Treatment
1 Other