FDA Adverse Event Malfunction Summary report: N

NON AC-POWERED PATIENT LIFT

MDR report key: 3211916 · Received July 8, 2013

Report

Report Number
1219590-2013-00055
Event Type
Malfunction
Date Received
July 8, 2013
Report Date
June 13, 2013
Manufacturer
INVACARE CLEVELAND STREET
Product Code
FSA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IN, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PROVIDER STATES WILL NOT LIFT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
309654 NON AC-POWERED PATIENT LIFT 880.5510 FSA INVACARE CLEVELAND STREET H605

Patients

Seq Age Sex Outcome Treatment
1 Other