Product Recall: Artis PL E and Artis Symbiose Intraocular Lenses

The ANSM has issued a safety alert regarding a product recall of Artis PL E and Artis Symbiose intraocular lenses, initiated by Cristalens Industrie. The recall is identified under ANSM safety action number R2606056. Healthcare facilities that received the associated notification letter are directly involved in this action.

Healthcare providers must immediately cease use of the affected intraocular lenses and follow the instructions provided by Cristalens Industrie. While no specific compliance deadline is stated, the nature of a product recall implies an immediate need for action to prevent patient harm. Further questions should be directed to the manufacturer.