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WARNING: RECALLED PRODUCT
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Oekolp forte

Exceeding the established limit of an unknown impurity was found in batch 23000333, making it impossible to assess safety of use. The authority indicated a real risk to patients’ health and potentially life. Potential effects: poisoning, serious adverse reactions, life‑threatening events.

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Oekolp forte
Risk Level
Critical
Manufacturer
Besins Healthcare Germany GmbH, Niemcy; importer równoległy: InPharm sp. z o.o., 03-138 Warszawa
Batch Number
23000333
EAN Code
05909997211268
Recall Date
13.05.2024
View official statement

Important Information

What You Should Know

Recommendations

Do not use the product from batch 23000333. Check the batch number on the packaging; if you have this batch, return it to the pharmacy. If the medicine has been used and any worrying symptoms occur, c...

Actions Taken

The Main Pharmaceutical Inspector withdrew batch 23000333 of Oekolp forte 0.5 mg vaginal pessaries from the entire Polish market, prohibited placing this batch on the market, and granted the decision ...

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 established limit of an unknown impurity was found in batch 23000333, making it impossible to assess safety of use. The authority indicated a real risk to patients’ health and potentially life. Potential effects: poisoning, serious adverse reactions, life‑threatening events.
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: 23000333

Related

Other Recalled Products