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WARNING: RECALLED PRODUCT
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RANITYDYNA AUROVITAS

Exceedance of the acceptable limit of N-nitrosodimethylamine (NDMA) contamination was detected and confirmed in products containing Ranitidinum, creating a real, high probability of a threat to patients’ health or life. Potential effects: chronic exposure, carcinogenic effects, liver damage, general poisoning of the body.

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RANITYDYNA AUROVITAS
Risk Level
Critical
Manufacturer
Aurovitas Pharma Polska Sp. z o.o.
Batch Number
NCSA18009-A, NCSA18010-A, NCSA18011-B, NCSA19002-B, NGSA19003-A, NCSA19004-A, NCS$A19009-A, NCSA19016-A, NCSA19017-A
Recall Date
11.10.2019
View official statement

Important Information

What You Should Know

Recommendations

Do not use the product from the listed batches. Patients should check the batch number of their medicine, stop using it, and consult a doctor or pharmacist regarding further treatment and possible ret...

Actions Taken

The Chief Pharmaceutical Inspector withdrew the specified batches of the medicinal product Ranitidine Aurovitas from the market throughout the country, granted the decision immediate enforceability, a...

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: Exceedance of the acceptable limit of N-nitrosodimethylamine (NDMA) contamination was detected and confirmed in products containing Ranitidinum, creating a real, high probability of a threat to patients’ health or life. Potential effects: chronic exposure, carcinogenic effects, liver damage, general poisoning of the body.
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: NCSA18009-A, NCSA18010-A, NCSA18011-B, NCSA19002-B, NGSA19003-A, NCSA19004-A, NCS$A19009-A, NCSA19016-A, NCSA19017-A

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