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WARNING: RECALLED PRODUCT
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EUREFIN

A risk of use of the medicinal product Eurefin disproportionate to its therapeutic effect was identified, meaning that the benefit–risk balance of medicines containing fenspiride is not favourable. Potential effects: serious adverse reactions, unacceptable safety profile, possible threat to patients’ health or life.

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EUREFIN
Risk Level
Critical
Manufacturer
Przedsiębiorstwo Produkcji Farmaceutycznej HASCO-LEK S.A.
Batch Number
wszystkie serie
Recall Date
22.08.2019
View official statement

Important Information

What You Should Know

Recommendations

Do not use Eurefin; patients should stop taking it, check the medicine name and, in case of doubt, contact a doctor or pharmacist.

Actions Taken

Temporary suspension and prohibition of placing all batches on the market, followed by revocation of the marketing authorisation and a decision of the Chief Pharmaceutical Inspector to withdraw Eurefi...

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: A risk of use of the medicinal product Eurefin disproportionate to its therapeutic effect was identified, meaning that the benefit–risk balance of medicines containing fenspiride is not favourable. Potential effects: serious adverse reactions, unacceptable safety profile, possible threat to patients’ health or life.
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: wszystkie serie

Related

Other Recalled Products