What does this decision mean?
Out-of-specification (OOS) results were found in retention samples for atomoxetine content and, for batch 1304011, also for mass uniformity; the impact of this non‑conformity on the drug’s efficacy and safety cannot be determined. Potential effects: reduced treatment efficacy or unpredictable adverse effects.
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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 Konaten capsules from the listed batches. Patients should check the batch number on the packaging, consult their doctor or pharmacist about further therapy, and, if appropriate, return the ...
The Chief Pharmaceutical Inspector suspended distribution of selected batches of Konaten (Atomoxetine), hard capsules throughout the country and granted the decision immediate enforceability.
If you feel unwell after consuming this product, contact your doctor or call the poison control center.