Recall of Femoral Extension Rod Mets Integral Coated Type Shaft and Stem Round (Orthopedics)

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 Stanmore Implants.

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.

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Device

Manufacturer

  • Manufacturer Parent Company (2017)
  • Source
    LAANSM