VBLAAST 10

GIF decision: Marketing prohibition

What does this decision mean?

  • Zakaz wprowadzania — Selected batches are subject to a marketing prohibition — the product cannot be distributed to pharmacies.

Visible particles of unidentified origin were found in the solution for injection, which creates a real risk of such particles entering the patient’s bloodstream and may lead to unpredictable, negative health effects. Potential effects: embolic complications, tissue damage, severe systemic complications.

Download the app and stay informed

Get instant notifications about recalled products and protect your family.

VBLAAST 10
Risk Level
Critical
Manufacturer
podmiot odpowiedzialny: VAMA LIFECARE PVT. LTD. z siedzibą w Indiach; podmiot, który uzyskał zgodę na czasowe dopuszczenie do obrotu: MEDYK-LEK Panek sp. z o.o. sp. k. z siedzibą w Warszawie
Batch Number
OI0774
Notice Date
27.05.2025
View official statement
Source: GIF view the official alert

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. 1

    Do not eat or use the product

    Stop using or consuming it immediately and keep it out of reach of children.

  2. 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. 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. 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 product from batch OI0774, check the batch number of vials on hand and return them to the pharmacy or wholesaler; if a dose from this batch was administered, monitor the patient and contact...

Actions Taken

The Chief Pharmaceutical Inspector withdrew batch OI0774 of VBLAAST 10 from the market nationwide, prohibited further placing of this batch on the market, granted the decision immediate enforceability...

Need Help?

If you feel unwell after consuming this product, contact your doctor or call the poison control center.

Related

Other Notices