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 to the naked eye crystals of unidentified origin were found in the medicinal product in the form of a solution for injection; their entry into the patient’s bloodstream may lead to unpredictable adverse health effects. Potential effects: vascular complications, organ damage, severe systemic complications.

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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 produktu leczniczego: Genesis Pharm sp. z o.o. sp. komandytowa, ul. Obywatelska 128/152, 94-104 Łódź.
Batch Number
I23I011B
Notice Date
09.02.2024
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 the product from batch I23I011B, check the batch number of any stock and return it to the pharmacy or wholesaler; if the product has been administered, consult a doctor.

Actions Taken

The Chief Pharmaceutical Inspector withdrew batch I23I011B of the product from the market nationwide, prohibited any further placing of this batch on the market, and granted the decision immediate enf...

Need Help?

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

Related

Other Notices