Recall of 2M insert 15 ° for MUTARS RS cup LUMiC TiN

According to National Organization for Medicines, this recall involved a device in Greece that was produced by Implantcast GmbH.

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

  • Model / Serial
  • Product Description
    Retrieval of specific codes for Category III medical devices 2M insert 15 ° for MUTARS RS cup & LUMiC TiN
  • Manufacturer

Manufacturer