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WARNING: RECALLED PRODUCT
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Taromentin

It was found that in the carton of Taromentin 1000 mg + 200 mg (batch 2010525) there was a vial of Taromentin 500 mg + 100 mg, containing half the dose of active substances, which may lead to insufficient therapeutic efficacy. Potential effects: lack of treatment efficacy, possible infection-related complications.

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Taromentin
Risk Level
Critical
Manufacturer
Tarchomińskie Zakłady Farmaceutyczne "Polfa" S.A. z siedzibą w Warszawie
Batch Number
2010525
Recall Date
30.01.2026
View official statement

FAQ

Frequently Asked Questions

Is this product safe to consume?
No. This product has been recalled due to: It was found that in the carton of Taromentin 1000 mg + 200 mg (batch 2010525) there was a vial of Taromentin 500 mg + 100 mg, containing half the dose of active substances, which may lead to insufficient therapeutic efficacy. Potential effects: lack of treatment efficacy, possible infection-related complications.
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.

Related

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