Furaginum MAX US Pharmacia

GIF decision: Re-authorization for marketing

What does this decision mean?

• Ponowne dopuszczenie do obrotu — The product has been re-authorized for marketing after earlier restrictions.

NIL testing showed that the product does not meet quality requirements due to a failed test for nitrosamine content: NDMA, indicating contamination of the product with a potentially carcinogenic compound. Potential effects: chronic exposure, increased cancer risk, possible other toxic effects.

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Risk Level

Critical

Manufacturer

US Pharmacia Sp. z o.o.

Batch Number

12872535

Notice Date

28.01.2026

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.

Furaginum MAX US Pharmacia

What to do if you have this product?

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