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WARNING: RECALLED PRODUCT
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Lakcid forte

It was found that the product sample does not comply with the specification regarding the number of lactic acid bacteria CFU, which may lead to reduced therapeutic effectiveness of the probiotic preparation. Potential effects: reduced treatment effectiveness, lack of the expected probiotic effect.

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Lakcid forte
Risk Level
Medium
Manufacturer
Zakłady Farmaceutyczne POLPHARMA S.A.
Batch Number
01518
EAN Code
05909990322725
Recall Date
06.11.2019
View official statement

Important Information

What You Should Know

Recommendations

Do not use the product from batch 01518, check the batch number on the packaging, and if you have this product, return it to a pharmacy; if you have any concerns about your treatment, consult a doctor...

Actions Taken

Withdrawal from the market throughout the country of batch 01518 of the medicinal product Lakcid forte, granting the decision immediate enforceability, and obliging the marketing authorisation holder ...

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 found that the product sample does not comply with the specification regarding the number of lactic acid bacteria CFU, which may lead to reduced therapeutic effectiveness of the probiotic preparation. Potential effects: reduced treatment effectiveness, lack of the expected probiotic effect.
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: 01518

Related

Other Recalled Products