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WARNING: RECALLED PRODUCT
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Konaten

Out-of-specification (OOS) results were found in retention samples for atomoxetine content and, for batch 1304011, also for mass uniformity; the impact of this non‑conformity on the drug’s efficacy and safety cannot be determined. Potential effects: reduced treatment efficacy or unpredictable adverse effects.

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Konaten
Risk Level
Medium
Manufacturer
neuraxpharm Arzneimittel GmbH z siedzibą w Niemczech
Batch Number
1300867
EAN Code
05909991390952
Recall Date
17.07.2024
View official statement

Important Information

What You Should Know

Recommendations

Do not use Konaten capsules from the listed batches. Patients should check the batch number on the packaging, consult their doctor or pharmacist about further therapy, and, if appropriate, return the ...

Actions Taken

The Chief Pharmaceutical Inspector suspended distribution of selected batches of Konaten (Atomoxetine), hard capsules throughout the country 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: Out-of-specification (OOS) results were found in retention samples for atomoxetine content and, for batch 1304011, also for mass uniformity; the impact of this non‑conformity on the drug’s efficacy and safety cannot be determined. Potential effects: reduced treatment efficacy or unpredictable adverse effects.
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: 1300867

Related

Other Recalled Products