FDA Adverse Event Malfunction Summary report: N

FGA 330 PORTABLE ALUMINUM LIFT 330 LBS

MDR report key: 5143574 · Received October 11, 2015

Report

Report Number
3007802293-2015-00041
Event Type
Malfunction
Date Received
October 11, 2015
Date of Event
September 17, 2015
Report Date
October 9, 2015
Manufacturer
PRISM MEDICAL
Product Code
FSA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Additional Manufacturer Narrative · 1

THE FGA 330 PORTABLE ALUMINUM LIFT HAS NOT BEEN RECEIVED TO EVALUATE. FOLLOWING RECEIPT AND INVESTIGATION OF THE DEVICE, THIS REPORT WILL BE UPDATED.

Description of Event or Problem · 1

LEG WELDMENT BREAK REPORTED BY END USER AT ACTUATOR POST ON FGA 330 PORTABLE ALUMINUM LIFT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
674146 FGA 330 PORTABLE ALUMINUM LIFT 330 LBS FGA 330 LIFT FSA PRISM MEDICAL 280420

Patients

Seq Age Sex Outcome Treatment
1