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WARNING: RECALLED PRODUCT
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Konaten

Testing of reference samples showed that the batches covered by the decision do not meet specifications for atomoxetine content, and batch 1311190 also fails the mass uniformity parameter. Potential effects: reduced treatment efficacy, variable dosing, possible therapy complications.

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Konaten
Risk Level
Medium
Manufacturer
Neuraxpharm Arzneimittel GmbH z siedzibą w Niemczech
Batch Number
1304010
EAN Code
05909991390938
Recall Date
28.05.2024
View official statement

Important Information

What You Should Know

Recommendations

Do not use Konaten capsules from the listed batches. Check the batch number on the pack; return any affected packs to the pharmacy and consult your doctor or pharmacist about continuing or adjusting t...

Actions Taken

The distribution of the listed batches of Konaten was suspended nationwide and the decision was given immediate enforceability; the manufacturer halted production of atomoxetine-containing products un...

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: Testing of reference samples showed that the batches covered by the decision do not meet specifications for atomoxetine content, and batch 1311190 also fails the mass uniformity parameter. Potential effects: reduced treatment efficacy, variable dosing, possible therapy complications.
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: 1304010

Related

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