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WARNING: RECALLED PRODUCT
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Febrisan

An out-of-specification result was found in stability testing: at 12 months the content limits for paracetamol and ascorbic acid were exceeded; it is uncertain whether the rest of the batch meets quality requirements for active substance content. Potential effects: reduced treatment efficacy or increased adverse effects.

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Febrisan
Risk Level
Medium
Manufacturer
Orifarm Healthcare A/S
Batch Number
100401
EAN Code
05909990864072
Recall Date
26.01.2023
View official statement

Important Information

What You Should Know

Recommendations

Do not use product from batch 100401; check the batch number and, if you have it, return the product to a pharmacy or consult a doctor.

Actions Taken

The medicinal product Febrisan, batch 100401, was withdrawn from the market throughout the country and the decision was given immediate enforceability.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: An out-of-specification result was found in stability testing: at 12 months the content limits for paracetamol and ascorbic acid were exceeded; it is uncertain whether the rest of the batch meets quality requirements for active substance content. Potential effects: reduced treatment efficacy or increased adverse effects.
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: 100401

Related

Other Recalled Products