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WARNING: RECALLED PRODUCT
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Lakcid forte

The test showed that the product sample does not comply with the specification regarding the CFU count of lactic acid bacteria (Lactobacillus rhamnosus), which may mean a lower content of live probiotic bacteria than declared. Potential effects: lack of treatment efficacy, possible worsening of symptoms, delay of therapy.

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Lakcid forte
Risk Level
Low
Manufacturer
Zakłady Farmaceutyczne POLPHARMA S.A.
Batch Number
010319
EAN Code
05909991067830
Recall Date
06.11.2019
View official statement

Important Information

What You Should Know

Recommendations

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

Actions Taken

The Chief Pharmaceutical Inspector withdrew the specified batch of the medicinal product from the market throughout the country and granted the decision immediate enforceability, obliging the marketin...

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: The test showed that the product sample does not comply with the specification regarding the CFU count of lactic acid bacteria (Lactobacillus rhamnosus), which may mean a lower content of live probiotic bacteria than declared. Potential effects: lack of treatment efficacy, possible worsening of symptoms, delay of therapy.
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: 010319

Related

Other Recalled Products