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WARNING: RECALLED PRODUCT
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Konaten

Out-of-specification results were found in reference samples for atomoxetine content (outside the 95.0–105.0% range) and, in one case, for capsule mass, indicating variable active substance dosage. Potential effects: reduced treatment effectiveness or increased adverse reactions.

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Konaten
Risk Level
Medium
Manufacturer
neuraxpharm Arzneimittel GmbH z siedzibą Niemczech
Batch Number
1111121
EAN Code
05909991390938
Recall Date
28.08.2024
View official statement

Important Information

What You Should Know

Recommendations

Do not use the medicine from the listed batches. Check the batch number on the package and, if it matches, return the product to the pharmacy or contact your doctor to obtain a replacement.

Actions Taken

The Pharmaceutical Inspector withdrew the specified batches of Konaten from the national market, prohibited their further placing on the market, and granted the decision immediate enforceability; prev...

Need Help?

If you feel unwell after consuming this product, contact your doctor or call the poison control center.

FAQ

Frequently Asked Questions

Is this product safe to consume?
No. This product has been recalled due to: Out-of-specification results were found in reference samples for atomoxetine content (outside the 95.0–105.0% range) and, in one case, for capsule mass, indicating variable active substance dosage. Potential effects: reduced treatment effectiveness or increased adverse reactions.
What should I do if I already bought this?
Stop using the product immediately. Return it to the store for a full refund. If you consumed it and feel unwell, contact your doctor.
Which batches are affected?
Affected batch numbers: 1111121

Related

Other Recalled Products