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WARNING: RECALLED PRODUCT
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Aribit

An out-of-specification result was obtained in long-term stability testing for the parameter: aripiprazole active substance content, confirming that the product does not meet quality requirements. Potential effects: lack of treatment efficacy or adverse effects related to an incorrect dose.

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Aribit
Risk Level
Medium
Manufacturer
Zakłady Farmaceutyczne POLPHARMA S.A. z siedzibą w Starogardzie Gdańskim
Batch Number
011020
EAN Code
05907529463383
Recall Date
12.10.2021
View official statement

Important Information

What You Should Know

Recommendations

Do not use Aribit 30 mg from batch 011020 with expiry date 10.2023. Check the batch number on the packaging and, if you have this batch, return the product to a pharmacy and consult a doctor if in dou...

Actions Taken

The Chief Pharmaceutical Inspector withdrew batch 011020 of Aribit 30 mg from the market throughout the country and granted the decision immediate enforceability.

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: An out-of-specification result was obtained in long-term stability testing for the parameter: aripiprazole active substance content, confirming that the product does not meet quality requirements. Potential effects: lack of treatment efficacy or adverse effects related to an incorrect dose.
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: 011020

Related

Other Recalled Products