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WARNING: RECALLED PRODUCT
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ZOLAXA RAPID

A quality defect was found: an out-of-specification result for the active substance content per tablet, which may mean an incorrect dose of the medicine for the patient. Potential effects: lack of treatment efficacy or increased adverse effects.

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ZOLAXA RAPID
Risk Level
High
Manufacturer
Zakłady Farmaceutyczne POLPHARMA S.A.
Batch Number
10518
Recall Date
29.08.2019
View official statement

Important Information

What You Should Know

Recommendations

Do not use the product from batch 10518, check the batch number on the packaging, and if you have this batch, return the product to the pharmacy or consult a doctor.

Actions Taken

Withdrawal from the market throughout the country of batch 10518 of the medicinal product Zolaxa Rapid and granting 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: A quality defect was found: an out-of-specification result for the active substance content per tablet, which may mean an incorrect dose of the medicine for the patient. Potential effects: lack of treatment efficacy or increased adverse effects.
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: 10518

Related

Other Recalled Products