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WARNING: RECALLED PRODUCT
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Angeliq

The medicinal product was released to the market with an outdated version of the patient leaflet; a health risk cannot be excluded due to information inconsistent with the approved documentation. Potential effects: incorrect use of the drug, lack of treatment efficacy, complications or increased adverse reactions.

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Angeliq
Risk Level
High
Manufacturer
Bayer AG z siedzibą w Leverkusen, Niemcy
Batch Number
KT0SLCS
EAN Code
05909990221073
Recall Date
18.04.2025
View official statement

Important Information

What You Should Know

Recommendations

Do not use the medicine from batch KT0SLCS. Patients should check the batch number on the packaging, return the product to the pharmacy if they have this batch, and consult a doctor or pharmacist for ...

Actions Taken

The Chief Pharmaceutical Inspector withdrew batch KT0SLCS of Angeliq from the market throughout the country and prohibited placing this batch on the market, granting the decision immediate enforceabil...

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No. This product has been recalled due to: The medicinal product was released to the market with an outdated version of the patient leaflet; a health risk cannot be excluded due to information inconsistent with the approved documentation. Potential effects: incorrect use of the drug, lack of treatment efficacy, complications 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: KT0SLCS

Related

Other Recalled Products