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WARNING: RECALLED PRODUCT
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Hemkortin-HC

Incorrect strength of the medicinal product was found on the immediate (tube) packaging, which may mislead patients or medical staff about the dose being used. Potential effects: improper dosing, lack of therapeutic efficacy or increased adverse reactions.

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Hemkortin-HC
Risk Level
High
Manufacturer
Polmex Pharma Biniecki & Malinowski Sp. j.
Batch Number
A0030
EAN Code
05909990353422
Recall Date
18.02.2021
View official statement

Important Information

What You Should Know

Recommendations

Do not use the ointment from batches A0030, B0131 and C0143. Check the batch number on the tube and, if you have a product from these batches, return it to the pharmacy or consult a doctor or pharmaci...

Actions Taken

The Chief Pharmaceutical Inspector withdrew the specified batches of Hemkortin-HC from the market throughout the country and granted the decision immediate enforceability, obliging the marketing autho...

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: Incorrect strength of the medicinal product was found on the immediate (tube) packaging, which may mislead patients or medical staff about the dose being used. Potential effects: improper dosing, lack of therapeutic efficacy or increased adverse reactions.
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: A0030

Related

Other Recalled Products