oAlert.pl
WARNING: RECALLED PRODUCT
PL EN

BDS N

Out-of-specification results were found for the content of related substances of budesonide, due to exceeded impurity levels. Potential effects: lack of treatment efficacy or adverse reactions caused by impurities.

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BDS N
Risk Level
Medium
Manufacturer
Apotex Europe B.V. z siedzibą w Holandii
Recall Date
17.07.2019
View official statement

Important Information

What You Should Know

Recommendations

Do not use the product from the withdrawn batches; patients should contact a pharmacist or physician to determine further treatment.

Actions Taken

The Chief Pharmaceutical Inspector decided to withdraw the specified batches of the medicinal product BDS N 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: Out-of-specification results were found for the content of related substances of budesonide, due to exceeded impurity levels. Potential effects: lack of treatment efficacy or adverse reactions caused by impurities.
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