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WARNING: RECALLED PRODUCT
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PALIN

The European Medicines Agency decision concerned serious adverse reactions of some quinolone and fluoroquinolone antibiotics; the benefit-risk balance of products containing pipemidic acid is no longer favorable. Potential effects: serious adverse reactions, complications, risk to health or life.

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PALIN
Risk Level
Critical
Manufacturer
Sandoz GmbH, Austria
Batch Number
ES9801
EAN Code
05909990172917
Recall Date
11.10.2019
View official statement

Important Information

What You Should Know

Recommendations

Do not use Palin capsules from the listed batches; patients currently taking this medicine should contact their doctor to consider changing therapy.

Actions Taken

The Chief Pharmaceutical Inspector withdrew all specified batches of Palin 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 European Medicines Agency decision concerned serious adverse reactions of some quinolone and fluoroquinolone antibiotics; the benefit-risk balance of products containing pipemidic acid is no longer favorable. Potential effects: serious adverse reactions, complications, risk to health or life.
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: ES9801

Related

Other Recalled Products