oAlert.pl
WARNING: RECALLED PRODUCT
PL EN

Liv 52

a medicinal product whose quality cannot be properly verified due to the company’s failure to update the documentation that serves as the reference point for assessing the product’s quality. Potential effects: lack of efficacy, unpredictable adverse reactions.

Download the app and stay informed

Get instant notifications about recalled products and protect your family.

Liv 52
Risk Level
Medium
Manufacturer
„World Markets” sp. z o.o. z siedzibą w Warszawie
Batch Number
112302614
EAN Code
05909990461714
Recall Date
13.03.2025
View official statement

Important Information

What You Should Know

Recommendations

Do not use Liv 52 from the listed batches. Check the batch number on the packaging and return any affected packs to a pharmacy or consult a doctor or pharmacist to determine further steps.

Actions Taken

The Chief Pharmaceutical Inspector withdrew the medicinal product Liv 52 in the specified 18 batches from the Polish market, prohibited placing this product on the market in all batches, and granted t...

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 medicinal product whose quality cannot be properly verified due to the company’s failure to update the documentation that serves as the reference point for assessing the product’s quality. Potential effects: lack of efficacy, unpredictable adverse reactions.
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: 112302614

Related

Other Recalled Products