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WARNING: RECALLED PRODUCT
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RANIC

Contamination of the medicinal product with trace amounts of N-nitrosodimethylamine (NDMA) in the ranitidine-containing solution for injection. Potential effects: carcinogenic and toxic effects, possible health risk.

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RANIC
Risk Level
Critical
Manufacturer
Sandoz GmbH, Austria
Batch Number
JE7613
EAN Code
05909990847419
Recall Date
18.10.2019
View official statement

Important Information

What You Should Know

Recommendations

Do not use the product from the listed batches; if in possession, return it to a pharmacy and, in case of doubts or worrying symptoms, consult a doctor.

Actions Taken

The Chief Pharmaceutical Inspector withdrew the specified batches of Ranic from the market throughout the country and granted 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: Contamination of the medicinal product with trace amounts of N-nitrosodimethylamine (NDMA) in the ranitidine-containing solution for injection. Potential effects: carcinogenic and toxic effects, possible 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?
Affected batch numbers: JE7613

Related

Other Recalled Products