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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; the altered capsule filling appearance does not match the currently registered quality specification. Potential effects: possible deviations in dosing and therapeutic effectiveness.

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Sunitinib Vipharm
Risk Level
Medium
Manufacturer
Vipharm S.A. z siedzibą w Ożarowie Mazowieckim
Batch Number
wszystkie serie (m.in. seria 4TY01A)
EAN Code
05901812162786
Recall Date
05.06.2025
View official statement

Important Information

What You Should Know

Recommendations

Do not use Sunitinib Vipharm due to the suspension of its marketing; patients should contact their doctor or pharmacist for an alternative medicine and further guidance.

Actions Taken

The marketing of all batches of Sunitinib Vipharm was suspended nationwide and the decision was given immediate enforceability; the product had previously been submitted for quality testing at the Nat...

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; the altered capsule filling appearance does not match the currently registered quality specification. Potential effects: possible deviations in dosing and therapeutic effectiveness.
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. seria 4TY01A)

Related

Other Recalled Products