Recall of Toptex® lite White Laparotomy compress with RX thread, 4-ply, 40 x 40 cm in the KP Grande Synthe / EN Cesarienne DE

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 Lohmann & Rauscher Laboratories SAS.

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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