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WARNING: RECALLED PRODUCT
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Nasen

A quality defect consisting in placing in the outer packaging of one medicinal product the blisters of another medicinal product, creating a risk that the patient will take the wrong medicine. Potential effects: inappropriate treatment, lack of therapeutic efficacy, serious adverse reactions.

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Nasen
Risk Level
High
Manufacturer
Polfarmex S.A.
Batch Number
020320
EAN Code
05909991187712
Recall Date
15.06.2020
View official statement

Important Information

What You Should Know

Recommendations

Do not use Furosemidum Polfarmex 40 mg and Nasen 10 mg from batch 020320. Check the batch number on the packaging and, if it matches, return the product to the pharmacy. If the wrong medicine has been...

Actions Taken

Batch 020320 of Furosemidum Polfarmex and Nasen was withdrawn from the market throughout the country, the decision was given immediate enforceability, and the marketing authorisation holder was oblige...

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: A quality defect consisting in placing in the outer packaging of one medicinal product the blisters of another medicinal product, creating a risk that the patient will take the wrong medicine. Potential effects: inappropriate treatment, lack of therapeutic efficacy, serious adverse reactions.
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: 020320

Related

Other Recalled Products