Menaright Forte, Phytomenadion Injection 2mg/0,2 ml

GIF decision: Withdrawal from market

What does this decision mean?

  • Wycofanie z obrotu — Some of the products covered by the decision were withdrawn from the market — please return them to the pharmacy/distributor.

The glass container shatters when opened, leaving glass fragments in the fingers and inside the ampoule, and differences in the solution volume in ampoules were found. Potential effects: injuries, glass foreign bodies, complications after injection, incorrect drug dose, life‑threatening events.

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Menaright Forte, Phytomenadion Injection 2mg/0,2 ml
Risk Level
Critical
Manufacturer
podmiot odpowiedzialny: Alvita Pharma Pvt. Ltd z siedzibą w Indiach, podmiot, który uzyskał zgodę na czasowe dopuszczenie do obrotu produktu leczniczego: IMPILO sp. z o.o. sp.k. z siedzibą w Będzinie
Batch Number
SH12032A
Notice Date
01.09.2022
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 SH12032A. Medical staff should immediately withdraw ampoules of this batch from use, return them to the wholesaler, and check batch numbers. In case of use and any injury...

Actions Taken

The Chief Pharmaceutical Inspector withdrew batch SH12032A of the medicinal product from the entire national market and granted the decision immediate enforceability, obliging the company to promptly ...

Need Help?

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

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