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WARNING: RECALLED PRODUCT
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Oxylaxon

In this case, the failure of the medicinal products to meet their specified quality requirement manifests as an excessively high content of one of the two active substances, i.e. oxycodone hydrochloride. Potential effects: opioid overdose, increased adverse reactions, risk to the patient’s health.

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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 medicine from the listed batches, check the batch number on the packaging and return the product to the pharmacy. If tablets from a defective batch have been taken, contact a doctor.

Actions Taken

The Chief Pharmaceutical Inspector withdrew specific batches of Oxylaxon from the market throughout the country and prohibited placing on the market all batches manufactured from granulate batch EE038...

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: In this case, the failure of the medicinal products to meet their specified quality requirement manifests as an excessively high content of one of the two active substances, i.e. oxycodone hydrochloride. Potential effects: opioid overdose, increased adverse reactions, risk to the patient’s health.
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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