Recall of Bacteriological reagents (including Vitek 2 ID, Vitek 2 AST, API Listeria), Vidas Toxo IgG avidity, Vidas FT4, Vidas anti-TPO

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 BIOMERIEUX SA.

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