What does this decision mean?
The National Medicines Institute found that the product does not meet quality requirements: in 6 of 68 capsules there were 9 mini-tablets instead of the required 10, meaning a reduced dose of active substance in some capsules. Potential effects: reduced treatment efficacy, risk of incomplete therapeutic response.
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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 the product from batch 23690003 (expiry date 09.2026). • Check the batch number and expiry date on the package before using the medicine. • If you have packs from this batch, consult a ph...
• The Chief Pharmaceutical Inspector withdrew the medicinal product Jaxteran 120 mg, gastro-resistant hard capsules, batch 23690003, from the market throughout Poland. • The placing on the market of t...
If you feel unwell after consuming this product, contact your doctor or call the poison control center.