Recall of Low Profile 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 Biomet 3i.

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
    R1609526
  • Date
    2016-09-23
  • 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
    ANSM has been informed of the implementation of a safety action / withdrawal of batch / withdrawal of product carried out by Biomet 3i. The users concerned have received the attached mail (23/09/2016) (148 KB). The following products are concerned (see references). Some low profile abutmen. Certain® low profile one-piece abutmen. Low profile abutmen. Low profile abutment (non-hexed) transfer printing copin. Low profile abutment healing CA. Low profile abutment non-hexed preformance® temporary cylinder. Low profile abutment pick-up print friend. Low profile abutment Quickbridge. Low profile abutment temporary cylinder. Low profile abutment titanium retaining scre. Low profile one-piece abutmen. This safety action is registered with the ANSM under the number R1609526.

Device

  • Model / Serial
  • Product Description
    medical_device
  • Manufacturer

Manufacturer

  • Manufacturer Parent Company (2017)
  • Manufacturer comment
    “The safety of patients has always been, and continues to be, Zimmer Biomet’s top priority and it is our honor to be a leader in this industry for the past 90 years,” Zimmer Biomet told ICIJ in a statement. “We adhere to strict regulatory standards, and work closely with the FDA and all applicable regulatory agencies in each of our regions as part of our commitment to operating a first-rate quality management system across our global manufacturing network. The company added that it is focused on staying at the forefront of innovation and doing right by the millions of patients who rely on the company’s products.
  • Source
    LAANSM