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WARNING: RECALLED PRODUCT
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Vblaast 10

Visible, unidentified crystals were found in the medicinal product in the form of an injection solution, creating a real danger of crystals entering the patient’s bloodstream and causing serious, unpredictable health consequences. Potential effects: thrombotic complications, vascular damage, embolism, 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
Recall Date
09.02.2024
View official statement

Important Information

What You Should Know

Recommendations

Do not use the medicine from this batch, check the batch number on the packaging, return the product to the pharmacy; if the medicine from this batch has been administered, contact a doctor immediatel...

Actions Taken

The Chief Pharmaceutical Inspector withdrew the specified batch of the medicinal product from the entire national market, prohibited its further placing on the market, and granted the decision immedia...

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: Visible, unidentified crystals were found in the medicinal product in the form of an injection solution, creating a real danger of crystals entering the patient’s bloodstream and causing serious, unpredictable health consequences. Potential effects: thrombotic complications, vascular damage, embolism, severe systemic complications.
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: I23I011B

Related

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