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WARNING: RECALLED PRODUCT
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Konaten

Out-of-specification (OOS) results were found for atomoxetine content (below the lower limit) and, for one batch, failure in capsule mass uniformity, which may lead to administration of too low a dose of the active substance. Potential effects: reduced treatment efficacy, possible worsening of disease symptoms.

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Konaten
Risk Level
Medium
Manufacturer
neuraxpharm Arzneimittel GmbH z siedzibą w Niemczech
Batch Number
1202428
EAN Code
05909991390952
Recall Date
28.08.2024
View official statement

Important Information

What You Should Know

Recommendations

Do not use the specified batches of Konaten, check the batch number on the packaging, return the product to the pharmacy, and if needed consult a doctor to ensure continuity of treatment with an alter...

Actions Taken

All listed batches of Konaten were withdrawn from the market throughout the country, their placing on the market was prohibited, and the decision was given immediate enforceability; previously, the di...

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 (OOS) results were found for atomoxetine content (below the lower limit) and, for one batch, failure in capsule mass uniformity, which may lead to administration of too low a dose of the active substance. Potential effects: reduced treatment efficacy, possible worsening of disease symptoms.
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: 1202428

Related

Other Recalled Products