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WARNING: RECALLED PRODUCT
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Hemkortin-HC

The product does not meet quality requirements due to a negative test result for the parameter “zinc sulfate monohydrate content”; the level of this substance was found below the lower limit specified in the quality specification. Potential effects: possible decreased treatment efficacy and incomplete drug action.

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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
27.01.2025
View official statement

Important Information

What You Should Know

Recommendations

Do not use the product from batch E0153; patients should check the batch number on the package and, if they have any doubts regarding their therapy, consult a doctor or pharmacist.

Actions Taken

Distribution of the medicinal product Hemkortin-HC, batch E0153, was suspended throughout the country after finding that it did not meet quality requirements; the decision was given immediate enforcea...

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 product does not meet quality requirements due to a negative test result for the parameter “zinc sulfate monohydrate content”; the level of this substance was found below the lower limit specified in the quality specification. Potential effects: possible decreased treatment efficacy and incomplete drug action.
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