Taromentin

GIF decision: Withdrawal from market, Marketing prohibition

What does this decision mean?

• Wycofanie z obrotu — Some of the products covered by the decision were withdrawn from the market — please return them to the pharmacy/distributor.
• Zakaz wprowadzania — Selected batches are subject to a marketing prohibition — the product cannot be distributed to pharmacies.

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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Risk Level

Critical

Manufacturer

Tarchomińskie Zakłady Farmaceutyczne "Polfa" S.A. z siedzibą w Warszawie

Batch Number

2010525

Notice Date

30.01.2026

What to do if you have this product?

A recall means the product may be unsafe. Here is what to do if you have it at home.

1

Do not eat or use the product

Stop using or consuming it immediately and keep it out of reach of children.
2

Check the batch number and expiry date

Compare the batch/lot number and the best-before or expiry date with the details in the alert — sometimes only specific batches are affected.
3

Return it to the shop

You can take the product back to the shop where you bought it. For a safety recall a refund is due even without a receipt.
4

Get help and report it

If you feel unwell after using the product, contact a doctor. You can also report the case to the relevant authority — GIS, GIF or UOKiK.

General guidance for recalled products in Poland. Always follow the specific instructions in the official alert and from the manufacturer or retailer.

Taromentin

What to do if you have this product?

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