Events

Recall of STRATEC MEDICAL USS FRACTURE SYSTEM - TI SCHANZ SCREW DUAL CORE

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
    38813
  • Event Risk Class
    II
  • Event Initiated Date
    2013-07-16
  • 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
    Synthes (canada) ltd. received notification from its supplier synthes gmbh that a medical device recall was being initiated for the transpedicular schanz screw dual core due to complaints received that the fracture clamp could not be used with the screw. in some cases the shaft of the screw is too thick.

Device

STRATEC MEDICAL USS FRACTURE SYSTEM - TI SCHANZ SCREW DUAL CORE
  • Model / Serial
    Model Catalog: 496.721 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 496.725 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 496.724 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 496.723 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 496.722 (Lot serial: >10 NUMBERS CONTACT MFG)
  • Product Description
    Titanium Transpedicular Schanz Screw Dual Core
  • Manufacturer
    SYNTHES (CANADA) LTD.

Manufacturer

SYNTHES (CANADA) LTD.
  • Manufacturer Address
    MISSISSAUGA
  • Manufacturer Parent Company (2017)
    Johnson & Johnson
  • Source
    HC