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WARNING: RECALLED PRODUCT
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ARTHRYL

The defect consists in the use of incorrect serialization data, resulting in incorrect identification of the medicinal product and failure to meet requirements for verification of authenticity and identification of the pack. Potential effects: possible use of an inappropriate or falsified drug, lack of treatment efficacy, treatment complications.

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ARTHRYL
Risk Level
Critical
Manufacturer
Mylan Healthcare Sp. z o.o.
Batch Number
0119P
Recall Date
07.06.2019
View official statement

Important Information

What You Should Know

Recommendations

Do not use the product from batch 0119P, check the batch number on the packaging and return the medicine to the pharmacy; if there are doubts about the taken preparation, consult a doctor or pharmacis...

Actions Taken

The Chief Pharmaceutical Inspector issued a decision to withdraw batch 0119P of Arthryl (400mg+10mg)/2ml, solution for injection, from the market with immediate enforceability; the marketing authoriza...

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 defect consists in the use of incorrect serialization data, resulting in incorrect identification of the medicinal product and failure to meet requirements for verification of authenticity and identification of the pack. Potential effects: possible use of an inappropriate or falsified drug, lack of treatment efficacy, treatment 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: 0119P

Related

Other Recalled Products