oAlert.pl
WARNING: RECALLED PRODUCT
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IRPRESTAN

Detection of N-nitrosodiethylamine (NDEA) above the acceptable limit in the active substance sourced from Zhejiang Huahai. Potential effects: carcinogenic action and long-term health risk.

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IRPRESTAN
Risk Level
Critical
Manufacturer
Actavis Group PTC ehf. z siedzibą w Islandii
Recall Date
24.01.2019
View official statement

Important Information

What You Should Know

Recommendations

Do not use medicine from this batch; check the batch number and return the product to the pharmacy; contact a doctor or pharmacist if in doubt.

Actions Taken

Withdrawal from the market of the specified batch of Irprestan 150 mg; decision by the Chief Pharmaceutical Inspector prohibiting placing the product on the market/withdrawing it with immediate enforc...

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: Detection of N-nitrosodiethylamine (NDEA) above the acceptable limit in the active substance sourced from Zhejiang Huahai. Potential effects: carcinogenic action and long-term 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