Recall of Distal attachment locking kits for external prosthesis 1S116, 1S117, 1S136 and 1S137

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 Proteor.

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

Device

  • Model / Serial
  • Product Description
    medical_device
  • Manufacturer

Manufacturer