Events

Recall of MYGO LECKEY WHEELCHAIR STANDER

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by JAMES LECKEY DESIGNS LTD.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    130385
  • Event Risk Class
    II
  • Event Initiated Date
    2016-08-04
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Extra notes in the data
  • Reason
    This correction (field safety corrective action) has been instigated by james leckey design ltd beacuse it is believed there is a remote risk of a hand/wrist injury to staff adjusting the angle of the mygo stander from a horizontal to a vertical positon. this risk can be eliminated through a simple correction.

Device

MYGO LECKEY WHEELCHAIR STANDER
  • Model / Serial
    Model Catalog: 143-2600 (Lot serial: >10 lots contact MFG); Model Catalog: 143-1600 (Lot serial: >10 lots contact MFG)
  • Product Description
    MYGO LECKEY Wheelchair Stander
  • Manufacturer
    JAMES LECKEY DESIGNS LTD

Manufacturer

JAMES LECKEY DESIGNS LTD