What does this decision mean?
A quality defect consisting in placing in the outer packaging of one medicinal product the blisters of another medicinal product, creating a risk that the patient will take the wrong medicine. Potential effects: inappropriate treatment, lack of therapeutic efficacy, serious adverse reactions.
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A recall means the product may be unsafe. Here is what to do if you have it at home.
Do not eat or use the product
Stop using or consuming it immediately and keep it out of reach of children.
Check the batch number and expiry date
Compare the batch/lot number and the best-before or expiry date with the details in the alert — sometimes only specific batches are affected.
Return it to the shop
You can take the product back to the shop where you bought it. For a safety recall a refund is due even without a receipt.
Get help and report it
If you feel unwell after using the product, contact a doctor. You can also report the case to the relevant authority — GIS, GIF or UOKiK.
General guidance for recalled products in Poland. Always follow the specific instructions in the official alert and from the manufacturer or retailer.
Important Information
Do not use Furosemidum Polfarmex 40 mg and Nasen 10 mg from batch 020320. Check the batch number on the packaging and, if it matches, return the product to the pharmacy. If the wrong medicine has been...
Batch 020320 of Furosemidum Polfarmex and Nasen was withdrawn from the market throughout the country, the decision was given immediate enforceability, and the marketing authorisation holder was oblige...
If you feel unwell after consuming this product, contact your doctor or call the poison control center.