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WARNING: RECALLED PRODUCT
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BUDIXON NEB

Exceedance of the specification limit for the content of budesonide-related substances was found for one batch and a probability of exceeding this limit for other batches of the product. Potential effects: lack of treatment efficacy or unpredictable adverse reactions.

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BUDIXON NEB
Risk Level
Medium
Manufacturer
Adamed Pharma S.A.
Batch Number
060218 oraz inne serie wymienione w decyzji (będące w terminie ważności)
EAN Code
05906414002782
Recall Date
01.08.2019
View official statement

Important Information

What You Should Know

Recommendations

Do not use the product from the withdrawn batches, check the batch number on the packaging and, if you have such a product, return it to the pharmacy or consult a doctor or pharmacist.

Actions Taken

The Chief Pharmaceutical Inspector decided to withdraw the specified batches of Budixon Neb 0.5 mg/ml from the market throughout the country and granted the decision immediate enforceability; the mark...

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 specification limit for the content of budesonide-related substances was found for one batch and a probability of exceeding this limit for other batches of the product. Potential effects: lack of treatment efficacy or unpredictable adverse 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?
Affected batch numbers: 060218 oraz inne serie wymienione w decyzji (będące w terminie ważności)

Related

Other Recalled Products