The defect consists in the use of incorrect serialization data, resulting in incorrect identification of the medicinal product and failure to meet requirements for verification of authenticity and identification of the pack. Potential effects: possible use of an inappropriate or falsified drug, lack of treatment efficacy, treatment complications.
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Important Information
Do not use the product from batch 0119P, check the batch number on the packaging and return the medicine to the pharmacy; if there are doubts about the taken preparation, consult a doctor or pharmacis...
The Chief Pharmaceutical Inspector issued a decision to withdraw batch 0119P of Arthryl (400mg+10mg)/2ml, solution for injection, from the market with immediate enforceability; the marketing authoriza...
If you feel unwell after consuming this product, contact your doctor or call the poison control center.
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