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WARNING: RECALLED PRODUCT
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Oxylaxon

The failure of the medicinal products to meet the established quality requirement manifests as an excessively high content of one of the two active substances, i.e. oxycodone hydrochloride. Potential effects: risk of overdose, poisoning, and increased opioid adverse effects.

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Oxylaxon
Risk Level
High
Manufacturer
G.L. Pharma GmbH, Schlossplatz 1, 8502 Lannach, Austria
Batch Number
E02215, F03209, F03210, E02270, F06046, F04680, E05198, E06924, F06611, F10132, F00149, E02249, E02259, F00148, E02261, F04703, F08633
Recall Date
27.11.2023
View official statement

Important Information

What You Should Know

Recommendations

Do not use the batches of the medicine covered by the decision. Patients should check the batch number of their Oxylaxon, and if it matches, return the medicine to the pharmacy and contact their docto...

Actions Taken

The Chief Pharmaceutical Inspector withdrew the specified batches of Oxylaxon from the market throughout the country and prohibited placing on the market all batches manufactured from granulate number...

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: The failure of the medicinal products to meet the established quality requirement manifests as an excessively high content of one of the two active substances, i.e. oxycodone hydrochloride. Potential effects: risk of overdose, poisoning, and increased opioid adverse effects.
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: E02215, F03209, F03210, E02270, F06046, F04680, E05198, E06924, F06611, F10132, F00149, E02249, E02259, F00148, E02261, F04703, F08633

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