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WARNING: RECALLED PRODUCT
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Megalia

Failure to meet quality requirements for the batch regarding microbiological purity, which poses a potential risk to patients’ health or life and was the basis for granting the decision immediate enforceability. Potential effects: infection, complications, lack of treatment safety.

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Megalia
Risk Level
High
Manufacturer
Vipharm S.A. z siedzibą w Ożarowie Mazowieckim
Batch Number
A981119
EAN Code
05909991054519
Recall Date
24.04.2020
View official statement

Important Information

What You Should Know

Recommendations

Do not use the product from this batch; check the batch number on the packaging and, if you have it, return the medicine to the pharmacy; in case of doubts, contact a doctor.

Actions Taken

The Chief Pharmaceutical Inspector withdrew batch A981119 of Megalia 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: Failure to meet quality requirements for the batch regarding microbiological purity, which poses a potential risk to patients’ health or life and was the basis for granting the decision immediate enforceability. Potential effects: infection, complications, 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: A981119

Related

Other Recalled Products