Recall of I-CONE (ICC) and HE Dental Implants

According to L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), this recall involved a device in France that was produced by Medical Production.

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
    201603252
  • Date
    2016-03-02
  • Event Country
  • Event Source
    ANSM
  • Event Source URL
  • Notes / Alerts
    French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), 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 France.
  • Extra notes in the data
  • Action
    The ANSM has been informed of the implementation of a product withdrawal carried out by the company MEDICAL PRODUCTION .. The users concerned have received the attached mail (02/03/2016) (103 KB). This safety action is registered with the ANSM under the number 201603252. You will be able to consult its progress status on the Directory of materiovigilance reports by entering this registration number. Read too. Decision of 11/02/2016 suspending the manufacture, placing on the market, export, distribution and use of dental implants of the references ICC (I-CONNE) and HE put on the market by the company MEDICAL PRODUCTION as well as withdrawal of these products (16/02/2016) (676 ko)

Device

Manufacturer