Vendal retard

GIF decision: Withdrawal from market, Marketing prohibition

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• Wycofanie z obrotu — Some of the products covered by the decision were withdrawn from the market — please return them to the pharmacy/distributor.
• Zakaz wprowadzania — Selected batches are subject to a marketing prohibition — the product cannot be distributed to pharmacies.

The medicinal product does not meet quality requirements: a single unknown impurity (related substances) was detected at a level exceeding the permitted limits in the product specification. Potential effects: possible alteration of drug effect or increased risk of adverse reactions.

Download the app and stay informed

Get instant notifications about recalled products and protect your family.

App Store Google Play

Risk Level

Medium

Manufacturer

G.L. Pharma GmbH

Batch Number

H01295

Notice Date

10.04.2026

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

Do not eat or use the product

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

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

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 Vendal retard 10 mg from batch H01295 originating from packs marked with GTIN 05909990743827. • Check the batch number on the pack; if you have batch H01295, consult your doctor or pharm...

Actions Taken

• The medicinal product Vendal retard (Morphine hydrochloride), 10 mg, prolonged-release film-coated tablets, pack of 30 tablets, GTIN 05909990743827, batch H01295, has been withdrawn from the market ...

Need Help?

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

Vendal retard

What to do if you have this product?

What You Should Know

Recommendations

Actions Taken

Need Help?

Other Notices

Magne B6

Ornispar

Viantan

Ornispar

TREC Nutrition CM3 products