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WARNING: RECALLED PRODUCT
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Ranimax Teva

In connection with information from the Rapid Alert system on detection of N-nitrosodimethylamine (NDMA) contamination in products containing ranitidine and the substantiated potential risk to patients’ health or life. Potential effects: long-term exposure to NDMA, possible carcinogenic action and other serious toxic effects.

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Ranimax Teva
Risk Level
Critical
Manufacturer
Teva Pharmaceuticals Polska Sp. z o.o.
Batch Number
010618
EAN Code
05909990144693
Recall Date
29.10.2019
View official statement

Important Information

What You Should Know

Recommendations

Do not use the product from the listed batches; check the batch number on the packaging and return the medicine to a pharmacy or consult a doctor about further treatment.

Actions Taken

Withdrawal from the market throughout the country of the specified batches of the medicinal product Ranimax Teva and granting the decision immediate enforceability, with an obligation for the marketin...

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: In connection with information from the Rapid Alert system on detection of N-nitrosodimethylamine (NDMA) contamination in products containing ranitidine and the substantiated potential risk to patients’ health or life. Potential effects: long-term exposure to NDMA, possible carcinogenic action and other serious toxic effects.
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: 010618

Related

Other Recalled Products