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WARNING: RECALLED PRODUCT
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Oxylaxon

A quality defect was identified consisting of an excessively high content of oxycodone hydrochloride in selected product batches, resulting from the use of granulate with incorrect quality parameters. Potential effects: opioid overdose, increased adverse reactions, respiratory depression, serious health complications.

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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 Oxylaxon tablets from the listed batches, check the batch number on the packaging, and if you have the product, return it to a pharmacy or consult a doctor; if symptoms of overdose occur, s...

Actions Taken

The Chief Pharmaceutical Inspector withdrew specific batches of the medicinal product Oxylaxon from the entire national market and prohibited placing on the market all batches manufactured from granul...

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: A quality defect was identified consisting of an excessively high content of oxycodone hydrochloride in selected product batches, resulting from the use of granulate with incorrect quality parameters. Potential effects: opioid overdose, increased adverse reactions, respiratory depression, serious health 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: E02215, F03209, F03210, E02270, F06046, F04680, E05198, E06924, F06611, F10132, F00149, E02249, E02259, F00148, E02261, F04703, F08633

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