Failure to meet quality requirements consists in ampoules being labeled as a different medicinal product with a higher strength, which may cause dosing mix‑ups and medication errors. Potential effects: lack of treatment efficacy or complications related to incorrect dosing.
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Important Information
Do not use the product from batch 054223, check the batch number on the packaging and return the medicine to the pharmacy; in case of doubts or adverse effects, contact a doctor.
The Chief Pharmaceutical Inspector withdrew batch 054223 of Benodil 0.25 mg/ml from the market nationwide and prohibited placing this batch on the market, granting the decision immediate enforceabilit...
If you feel unwell after consuming this product, contact your doctor or call the poison control center.
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