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WARNING: RECALLED PRODUCT
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PRESARTAN H

Detected nitrosamine-group impurities (NDMA and NDEA) in the active substance losartan potassium, which may affect human health and life, even though the levels do not exceed acceptable limits. Potential effects: possible carcinogenic effects and health complications with long-term use.

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PRESARTAN H
Risk Level
Critical
Manufacturer
PharmaSwiss Česká republika s.r.o., Republika Czeska
Recall Date
12.03.2019
View official statement

Important Information

What You Should Know

Recommendations

Do not use products containing losartan potassium from the contaminated series/manufacturer; verify batch information at the pharmacy or with your doctor; if in doubt, consult a physician to select an...

Actions Taken

The Chief Pharmaceutical Inspector decided to withdraw from the market medicinal products containing losartan potassium contaminated with NDMA and NDEA and granted the decision immediate enforceabilit...

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: Detected nitrosamine-group impurities (NDMA and NDEA) in the active substance losartan potassium, which may affect human health and life, even though the levels do not exceed acceptable limits. Potential effects: possible carcinogenic effects and health complications with long-term use.
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.

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