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WARNING: RECALLED PRODUCT
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RIFLUX

Suspected presence of N-nitrosodimethylamine (NDMA) contamination in medicinal products containing ranitidine, which may affect human health and life due to the potential toxic effects of this substance. Potential effects: possible toxic effects, complications, health risk.

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RIFLUX
Risk Level
Critical
Manufacturer
Polfarmex S.A.
Recall Date
19.09.2019
View official statement

Important Information

What You Should Know

Recommendations

Do not use medicinal products containing ranitidine, check the composition of medicines in use, and consult a doctor or pharmacist in case of doubts.

Actions Taken

Preventive suspension from the market of all medicinal products containing ranitidine and granting the decision 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: Suspected presence of N-nitrosodimethylamine (NDMA) contamination in medicinal products containing ranitidine, which may affect human health and life due to the potential toxic effects of this substance. Potential effects: possible toxic effects, complications, health risk.
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?
Check the official report for specific batch details.

Related

Other Recalled Products