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WARNING: RECALLED PRODUCT
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Atofab

Results out of specification (OOS) for atomoxetine content and non-uniformity of capsule mass in identified batches. Potential effects: reduced therapeutic efficacy.

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Atofab
Risk Level
Medium
Manufacturer
G.L. Pharma GmbH z siedzibą w Austrii
Batch Number
E01580
EAN Code
09008732012224
Recall Date
20.09.2024
View official statement

Important Information

What You Should Know

Recommendations

Do not use products from the listed batches; return to the point of sale or follow official guidance; check the batch number and contact a doctor if concerned.

Actions Taken

Withdrawal of the specified batches from nationwide distribution; ban on placing these batches on the market; prior suspension of distribution and initiation of administrative proceedings; decision ef...

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: Results out of specification (OOS) for atomoxetine content and non-uniformity of capsule mass in identified batches. Potential effects: reduced therapeutic efficacy.
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: E01580

Related

Other Recalled Products