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WARNING: RECALLED PRODUCT
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Andepin

Due to the detected increased content of a single impurity, a health risk for the patient taking this product cannot be excluded. Potential effects: poisoning, increased adverse reactions, complications of therapy.

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Andepin
Risk Level
Medium
Manufacturer
Przedsiębiorstwo Farmaceutyczno-Chemiczne "Synteza" Sp. z o.o., ul. Św. Michała 67/71, 61-005 Poznań
Batch Number
031122
EAN Code
05909991065515
Recall Date
24.07.2023
View official statement

Important Information

What You Should Know

Recommendations

Do not use Andepin with batch number 031122; if you have a pack, return it to the pharmacy and consult a doctor or pharmacist if in doubt.

Actions Taken

Withdrawal from the market across the entire country of Andepin batch 031122 due to a quality defect (chromatographic purity) and granting the decision immediate enforceability; the marketing authoris...

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: Due to the detected increased content of a single impurity, a health risk for the patient taking this product cannot be excluded. Potential effects: poisoning, increased adverse reactions, complications of therapy.
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: 031122

Related

Other Recalled Products