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WARNING: RECALLED PRODUCT
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BUDIXON NEB

Exceeding the specification limit for the parameter of budesonide-related substances was found for batch 060218 and a probability of exceeding the limit for other in-date batches. 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, inne serie będące w terminie ważności (niewymienione z nazwy)
EAN Code
05906414002539
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Do not use the product from the withdrawn batches; check the batch number on the packaging and, if you have such packs, return them to the pharmacy or manufacturer; in case of doubt, contact a doctor ...

Actions Taken

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

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: Exceeding the specification limit for the parameter of budesonide-related substances was found for batch 060218 and a probability of exceeding the limit for other in-date batches. 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, inne serie będące w terminie ważności (niewymienione z nazwy)

Related

Other Recalled Products