oAlert.pl
WARNING: RECALLED PRODUCT
PL EN

POLIPARIN 25000 IU/5 ml, Heparin sodium, solution for injection and infusion, 25000 IU/5 ml, 5 ml x 1 vial

Non‑compliances were observed involving “nodular clotting after administration of the product in several patients”, with no confirmed cause, which may directly lead to negative health consequences for patients. Potential effects: thrombosis, vascular complications, health risk.

Download the app and stay informed

Get instant notifications about recalled products and protect your family.

POLIPARIN 25000 IU/5 ml, Heparin sodium, solution for injection and infusion, 25000 IU/5 ml, 5 ml x 1 vial
Risk Level
Critical
Batch Number
E38310003A
Recall Date
17.09.2025
View official statement

Important Information

What You Should Know

Recommendations

Do not use POLIPARIN medicinal product from batch E38310003A (expiry 31.08.2026); check the batch number before use; if the product has been administered, consider consulting a physician.

Actions Taken

The Chief Pharmaceutical Inspector suspended the distribution of POLIPARIN 25000 IU/5 ml, batch E38310003A, throughout the country and granted the decision immediate enforceability; the company was ob...

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: Non‑compliances were observed involving “nodular clotting after administration of the product in several patients”, with no confirmed cause, which may directly lead to negative health consequences for patients. Potential effects: thrombosis, vascular complications, health risk.
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.

Related

Other Recalled Products