Recall of MATRIX THREADED PERSUADER

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by SYNTHES (CANADA) 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
    51950
  • Event Risk Class
    II
  • Event Initiated Date
    2013-06-20
  • Event Country
  • 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
    Synthes (canada) ltd. received notification from its supplier synthes usa that a medical device recall was being initiated for the matrix threaded persuader part number 03.632.008. this recall is being initiated as synthes has become aware that during a procedure using the matrix threaded persuader the reduction insert malfunctioned which caused pieces to break off. once there is breakage to the reduction insert it will not allow the instrument to function as required. the breakage of the insert represents the potential for an un-retrieved device fragment.

Device

  • Model / Serial
    Model Catalog: 03.632.008 (Lot serial: ALL LOTS)
  • Product Description
    MATRIX THREADED PERSUADER
  • Manufacturer

Manufacturer

  • Manufacturer Address
    MISSISSAUGA
  • Manufacturer Parent Company (2017)
  • Source
    HC