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WARNING: RECALLED PRODUCT
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Konaten

In reference samples, out-of-specification (OOS) results were found for atomoxetine content, and for batch 1304011 also for capsule mass uniformity, which may affect dosing. Potential effects: reduced treatment efficacy or adverse reactions due to incorrect dose.

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Konaten
Risk Level
Medium
Manufacturer
neuraxpharm Arzneimittel GmbH z siedzibą w Niemczech
Batch Number
1300918
EAN Code
05909991390990
Recall Date
17.07.2024
View official statement

Important Information

What You Should Know

Recommendations

Do not use products from the listed batches; check the batch number of any packs you have and, if applicable, consult a doctor or pharmacist and return the product to the pharmacy.

Actions Taken

The Chief Pharmaceutical Inspector suspended distribution throughout the country of the specified batches of Konaten and granted the decision immediate enforceability.

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: In reference samples, out-of-specification (OOS) results were found for atomoxetine content, and for batch 1304011 also for capsule mass uniformity, which may affect dosing. Potential effects: reduced treatment efficacy or adverse reactions due to incorrect dose.
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: 1300918

Related

Other Recalled Products