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WARNING: RECALLED PRODUCT
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Kidofen

Exceedance of the quality specification limit for the single impurity parameter was found, which may affect the effectiveness and safety of the medicine; a risk to children’s health cannot be excluded. Potential effects: possible adverse reactions, lack of efficacy, complications in children.

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Kidofen
Risk Level
Medium
Manufacturer
Aflofarm Farmacja Polska Sp. z o.o.
Batch Number
01AF1024
Recall Date
13.10.2025
View official statement

Important Information

What You Should Know

Recommendations

Do not use Kidofen 60 mg suppositories from batches 01AF1024 and 02AF1024. Check the batch number on the packaging and return products from these batches to a pharmacy. If the medicine has been used a...

Actions Taken

The Kidofen 60 mg suppository batches 01AF1024 and 02AF1024 were withdrawn from the market nationwide, placing these batches on the market was prohibited, the decision was given immediate enforceabili...

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: Exceedance of the quality specification limit for the single impurity parameter was found, which may affect the effectiveness and safety of the medicine; a risk to children’s health cannot be excluded. Potential effects: possible adverse reactions, lack of efficacy, complications in children.
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.

Related

Other Recalled Products