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WARNING: RECALLED PRODUCT
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Acurenal

It was determined that batches 80219782 and 80212781 do not meet the requirements for the parameter “Purity: content of impurity A”, and exceeding the acceptance criteria was considered a real and direct threat to patients’ health or life. Potential effects: possible adverse effects, poisoning, lack of treatment safety.

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Acurenal
Risk Level
Medium
Manufacturer
Bausch Health Ireland Limited z siedzibą w Irlandii
Batch Number
80219782
EAN Code
05909991125615
Recall Date
09.08.2024
View official statement

Important Information

What You Should Know

Recommendations

Do not use the product from batches 80219782 and 80212781. Patients should check the batch number on the packaging and, if they have these batches, return the medicine to a pharmacy and consult a doct...

Actions Taken

Distribution of Acurenal (Quinaprilum), film-coated tablets, batches 80219782 and 80212781 has been suspended throughout the country, the decision was given immediate enforceability, and the marketing...

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: It was determined that batches 80219782 and 80212781 do not meet the requirements for the parameter “Purity: content of impurity A”, and exceeding the acceptance criteria was considered a real and direct threat to patients’ health or life. Potential effects: possible adverse effects, poisoning, lack of treatment safety.
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: 80219782

Related

Other Recalled Products