Events

Recall of Micro-connector needle electrodes from BIOMEDIS

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 BIOMEDIS.

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
  • Date
    2002-01-24
  • Event Country
    France
  • Event Source
    ANSM
  • Event Source URL
    https://ansm.sante.fr/S-informer/Informations-de-securite-Retraits-de-lots-et-de-produits/retrait-d-electrodes-aiguilles-micro-connecteurs-de-la-societe-biomedis
  • 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
    All batches of micro-connector needle electrodes reference 034AMB001 BIOMEDIS whose expiry is less than or equal to March 30, 2003 were withdrawn from the market following the validation of the sterilization .. Given the small number of recipients of these devices, these have been warned directly by the manufacturer. As a result, no alert number has been assigned to this withdrawal.

Device

Micro-connector needle electrodes from BIOMEDIS
  • Model / Serial
  • Product Description
    medical_device
  • Manufacturer
    BIOMEDIS

Manufacturer

BIOMEDIS
  • Source
    LAANSM