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WARNING: RECALLED PRODUCT
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Febrisan

A quality defect was found consisting of micro-damages in the structure of the primary packaging foil, which may lead to loss of tightness and deterioration of the medicine’s quality. Potencjalne skutki: reduced treatment efficacy or adverse reactions.

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Febrisan
Risk Level
Medium
Manufacturer
Takeda Pharma Sp. z o.o., ul. Prosta 68, 00-838 Warszawa
Batch Number
450549
EAN Code
05909990864072
Recall Date
26.03.2021
View official statement

Important Information

What You Should Know

Recommendations

Do not use the product from the listed batches. If you have it, return the package to a pharmacy. If you have taken the medicine from a defective batch and experience worrying symptoms, contact a doct...

Actions Taken

The Chief Pharmaceutical Inspector withdrew the specified batches of Febrisan from the market nationwide and granted the decision immediate enforceability; the marketing authorisation holder was oblig...

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 quality defect was found consisting of micro-damages in the structure of the primary packaging foil, which may lead to loss of tightness and deterioration of the medicine’s quality. Potencjalne skutki: reduced treatment efficacy or 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: 450549

Related

Other Recalled Products