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WARNING: RECALLED PRODUCT
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Vblaast 10

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
Recall Date
09.02.2024
View official statement

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.

FAQ

Frequently Asked Questions

Is this product safe to consume?
No. This product has been recalled due to: 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.
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

Other Recalled Products