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WARNING: RECALLED PRODUCT
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Arpixor

The abnormal appearance of the tablets does not meet the product’s quality requirements and may lead to interruption of pharmacotherapy, which in turn may pose a risk to patients’ life or health. Potential effects: worsening of the disease, complications, risk to life or health.

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Arpixor
Risk Level
Medium
Manufacturer
neuraxpharm Arzneimittel GmbH
Batch Number
P1
EAN Code
05909991404710
Recall Date
25.08.2021
View official statement

Important Information

What You Should Know

Recommendations

Do not use Arpixor tablets from batch P1 with expiry date 06.2023; patients should check the batch number and, if they have this product, contact a pharmacist or doctor to return it and arrange approp...

Actions Taken

The Chief Pharmaceutical Inspector withdrew batch P1 of Arpixor from the market throughout the country and granted the decision immediate enforceability.

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 abnormal appearance of the tablets does not meet the product’s quality requirements and may lead to interruption of pharmacotherapy, which in turn may pose a risk to patients’ life or health. Potential effects: worsening of the disease, complications, risk to life or 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: P1

Related

Other Recalled Products