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WARNING: RECALLED PRODUCT
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Benodil

Failure to meet quality requirements consists in ampoules being labeled as a different medicinal product with a higher strength, which may cause dosing mix‑ups and medication errors. Potential effects: lack of treatment efficacy or complications related to incorrect dosing.

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Benodil
Risk Level
High
Manufacturer
Zakłady Farmaceutyczne POLPHARMA S.A., Starogard Gdański
Batch Number
054223
EAN Code
05903060614284
Recall Date
17.11.2023
View official statement

Important Information

What You Should Know

Recommendations

Do not use the product from batch 054223, check the batch number on the packaging and return the medicine to the pharmacy; in case of doubts or adverse effects, contact a doctor.

Actions Taken

The Chief Pharmaceutical Inspector withdrew batch 054223 of Benodil 0.25 mg/ml from the market nationwide and prohibited placing this batch on the market, granting 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: Failure to meet quality requirements consists in ampoules being labeled as a different medicinal product with a higher strength, which may cause dosing mix‑ups and medication errors. Potential effects: lack of treatment efficacy or complications related to incorrect dosing.
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: 054223

Related

Other Recalled Products