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WARNING: RECALLED PRODUCT
PL EN

BUDIXON NEB

Exceeding of specification limits for the content of budesonide related substances was found for batch 060218, with a probability of exceeding the limit for other batches still within shelf-life. Potential effects: lack of treatment efficacy, 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
05906414002775
Recall Date
01.08.2019
View official statement

Important Information

What You Should Know

Recommendations

Do not use the product from the specified batches, check the batch number on the packaging and, if you have it, return the medicine to the pharmacy; in case of doubts contact a doctor or pharmacist.

Actions Taken

The Chief Pharmaceutical Inspector withdrew the specified batches of the medicinal product Budixon Neb 0.5 mg/ml from the market throughout the country and granted the decision immediate enforceabilit...

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 of specification limits for the content of budesonide related substances was found for batch 060218, with a probability of exceeding the limit for other batches still within shelf-life. Potential effects: lack of treatment efficacy, 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