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WARNING: RECALLED PRODUCT
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Hemkortin-HC

The non-compliance indicated by OMCL may affect the quality of this product and the safety of its use, and therefore a risk to human health from keeping this batch of the medicinal product on the market cannot be excluded. Potential effects: lack of treatment efficacy, possible complications of the underlying disease.

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Hemkortin-HC
Risk Level
Medium
Manufacturer
POLMEX PHARMA BINIECKI SPÓŁKA KOMANDYTOWA z siedzibą w Warszawie
Batch Number
E0153
EAN Code
05909990353422
Recall Date
26.02.2025
View official statement

Important Information

What You Should Know

Recommendations

Do not use Hemkortin-HC ointment from batch E0153, check the batch number on the packaging, and return any packages to a pharmacy or consult a doctor or pharmacist.

Actions Taken

Withdrawal of batch E0153 of Hemkortin-HC from the entire national market and a ban on placing this batch on the market, with the decision 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: The non-compliance indicated by OMCL may affect the quality of this product and the safety of its use, and therefore a risk to human health from keeping this batch of the medicinal product on the market cannot be excluded. Potential effects: lack of treatment efficacy, possible complications of the underlying disease.
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: E0153

Related

Other Recalled Products