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WARNING: RECALLED PRODUCT
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Sunitinib Vipharm

The product does not meet quality requirements due to a negative test result for the “appearance” parameter – altered appearance of the capsule filling compared with the approved specification. Potential effects: possible non‑compliance of therapy with documentation and uncertainty regarding treatment quality.

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Sunitinib Vipharm
Risk Level
Low
Manufacturer
Vipharm S.A. z siedzibą w Ożarowie Mazowieckim
Batch Number
wszystkie serie (m.in. 4TW01A)
EAN Code
05901812162762
Recall Date
05.06.2025
View official statement

Important Information

What You Should Know

Recommendations

Do not use the product due to the identified quality non‑conformity; patients should consult their doctor or pharmacist about further treatment and check the name and batch of their medicine.

Actions Taken

The distribution of all batches of the medicinal product Sunitinib Vipharm 12.5 mg has been suspended throughout the country; the decision was given immediate enforceability; the product was sent for ...

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: The product does not meet quality requirements due to a negative test result for the “appearance” parameter – altered appearance of the capsule filling compared with the approved specification. Potential effects: possible non‑compliance of therapy with documentation and uncertainty regarding treatment quality.
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: wszystkie serie (m.in. 4TW01A)

Related

Other Recalled Products