FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3941305 · Received July 17, 2014

Report

Report Number
1031452-2014-03711
Event Type
Malfunction
Date Received
July 17, 2014
Report Date
June 11, 2014
Manufacturer
INVACARE CANADA KIRKLAND
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

IT WAS REPORTED THAT THE CAM LOCK BROKE ON THE MYONAC WHEELCHAIR.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
418485 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVACARE CANADA KIRKLAND MYONAC

Patients

Seq Age Sex Outcome Treatment
1 Other