Arpixor

Q: Is this product safe to consume?

No. This product has been recalled due to: According to the MAH’s representative, there is a justified suspicion that the Arpixor 30 mg, 56 tablets batch does not meet quality requirements regarding appearance. Potential effects: lack of treatment effectiveness or unpredictable drug action.

According to the MAH’s representative, there is a justified suspicion that the Arpixor 30 mg, 56 tablets batch does not meet quality requirements regarding appearance. Potential effects: lack of treatment effectiveness or unpredictable drug action.

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Risk Level

Medium

Manufacturer

neuraxpharm Arzneimittel GmbH

Batch Number

EAN Code

05909991404727

Recall Date

27.08.2021

What You Should Know

Recommendations

Do not use Arpixor 30 mg from batch P1. Patients who have this product should return it to a pharmacy and, in case of doubts, consult a doctor or pharmacist.

Actions Taken

The Chief Pharmaceutical Inspector withdrew Arpixor 30 mg, batch P1, 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: According to the MAH’s representative, there is a justified suspicion that the Arpixor 30 mg, 56 tablets batch does not meet quality requirements regarding appearance. Potential effects: lack of treatment effectiveness or unpredictable drug action.

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

Arpixor

What You Should Know

Recommendations

Actions Taken

Need Help?

Frequently Asked Questions

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