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WARNING: RECALLED PRODUCT
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FLUCINAR N

Out-of-specification result in a reference sample — impurities originating from fluocinolone acetonide. Potential effects: reduced efficacy, skin adverse effects (irritation, allergic reactions).

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FLUCINAR N
Risk Level
High
Manufacturer
Valeant Pharma Poland Sp. z o.o.
Recall Date
04.01.2019
View official statement

Important Information

What You Should Know

Recommendations

Do not use the product from the affected batch; return it to the pharmacy or manufacturer; check the batch number; contact a physician if you experience concerning symptoms.

Actions Taken

Decision to withdraw the batch of FLUCINAR N from the market with immediate enforceability; the marketing authorization holder is obliged to take legally required actions (notifications, recall).

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: Out-of-specification result in a reference sample — impurities originating from fluocinolone acetonide. Potential effects: reduced efficacy, skin adverse effects (irritation, allergic reactions).
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?
Check the official report for specific batch details.

Related

Other Recalled Products