Recall of Excelsior Microcatheters, GDC Coils, Neuroform EZ Stents and Transform Balloons (Neuroradiology)

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 STRYKER.

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



  • Manufacturer Parent Company (2017)
  • Source