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WARNING: RECALLED PRODUCT
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Konaten

Tests of reference samples showed that the batches covered by the decision do not meet the requirements for atomoxetine content, and batch 1311190 also fails the uniformity of mass parameter, which poses a real and direct risk to patients’ health. Potential effects: reduced treatment efficacy, risk of symptom worsening, possible complications resulting from improper dosing.

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Konaten
Risk Level
Medium
Manufacturer
Neuraxpharm Arzneimittel GmbH z siedzibą w Niemczech
Batch Number
1400775
EAN Code
05909991390952
Recall Date
28.05.2024
View official statement

Important Information

What You Should Know

Recommendations

Do not use the specified batches of the medicine; check the batch number on the packaging and, if you have the product, return it to the pharmacy and consult a doctor or pharmacist.

Actions Taken

Distribution of the specified batches of Konaten was suspended throughout the country and the decision was given 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: Tests of reference samples showed that the batches covered by the decision do not meet the requirements for atomoxetine content, and batch 1311190 also fails the uniformity of mass parameter, which poses a real and direct risk to patients’ health. Potential effects: reduced treatment efficacy, risk of symptom worsening, possible complications resulting from improper dosing.
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: 1400775

Related

Other Recalled Products