Recall of BD Perisafe and Durasafe kits

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 BECTON DICKINSON.

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
  • Date
  • Event Country
  • Event Source
  • 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    The company BECTON DICKINSON has withdrawn from the market on November 28, 2005, the references and batches specified in the appendix of the medical devices called "BD Perisafe kits and BD Durasafe kits" following some defective batches of connectors contained in these kits and which could lead to a problem of screwing. These kits are devices for epidural anesthesia. The company has directly notified the recipients of the incriminated lots with the message attached (28/11/2005) (25 KB) validated by the Afssaps. This information is addressed to the directors of health facilities, pharmacists and local vigilance correspondents for dissemination, where appropriate to the services concerned. The competent European authorities concerned shall be informed of this measure by the manufacturer.


  • Model / Serial
  • Product Description
  • Manufacturer