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WARNING: RECALLED PRODUCT
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Angeliq

It was found that an outdated version of the patient leaflet was included with batch KT0SLCS, so information on use, safety and adverse reactions does not meet current requirements. Potential effects: improper use of the medicine, lack of efficacy, increased risk of adverse reactions or complications.

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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 product from batch KT0SLCS; check the batch number on the packaging, and if you have this batch, return it to the pharmacy and consult a doctor or pharmacist if in doubt.

Actions Taken

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

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No. This product has been recalled due to: It was found that an outdated version of the patient leaflet was included with batch KT0SLCS, so information on use, safety and adverse reactions does not meet current requirements. Potential effects: improper use of the medicine, lack of efficacy, increased risk of adverse reactions or complications.
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