FDA Adverse Event Malfunction Summary report: N

NON AC-POWERED PATIENT LIFT

MDR report key: 3230701 · Received July 16, 2013

Report

Report Number
3004493922-2013-01516
Event Type
Malfunction
Date Received
July 16, 2013
Report Date
June 25, 2013
Manufacturer
INVACARE SUZHOU
Product Code
FSA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

THE PROVIDER STATED THE CASTER IS BROKEN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
328164 NON AC-POWERED PATIENT LIFT 880.5510 FSA INVACARE SUZHOU 9805P

Patients

Seq Age Sex Outcome Treatment
1 Other