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

GIF decision: Marketing suspension

What does this decision mean?

• Wstrzymanie w obrocie — The product has been temporarily suspended from circulation — sales are paused pending clarification, but it is not a full market recall.

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.

App Store Google Play

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

Notice Date

17.09.2025

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.

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.

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

What to do if you have this product?

What You Should Know

Recommendations

Actions Taken

Need Help?

Other Notices

Teicoplanin AptaPharma

Teicoplanin AptaPharma

Azaneson

Imuldosa

Loperamid APTEO MED