Recall of BD Whitacre and BD Yale 25G spinal needles

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
    Recall
  • Date
    2005-04-15
  • 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
    Following an error in his message broadcast on April 11, 200, concerning the withdrawal of lots of BD Whitacre and BD Yale 25G spinal needles, the company BECTON DICKINSON informs, in agreement with Afssaps, that the references and lots indicated -After are also concerned by this reminder: reference 405234 lot 406280. reference 409442 lot 411027. The attached message (11/04/2005) (25 KB) has been returned to the addressees concerned.

Device

  • Model / Serial
  • Product Description
    medical_device
  • Manufacturer

Manufacturer