The occurrence of incorrect information on the outer packaging regarding the repackaging site and the name of the parallel importer was classified as a quality defect of the medicinal product. Potential effects: incorrect use of the drug, inability to identify the responsible entity, possible therapy complications.
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Important Information
Do not use the product from this batch, check the batch number on the packaging and, if it matches, return the product to the pharmacy or consult a pharmacist or doctor.
The Chief Pharmaceutical Inspector withdrew the indicated batch of the medicinal product from the market throughout the country and granted the decision immediate enforceability; the responsible entit...
If you feel unwell after consuming this product, contact your doctor or call the poison control center.
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