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WARNING: RECALLED PRODUCT
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Adrimax

Localized turbidity of the Adrimax syrup solution detected in archived packages, indicating non-conforming appearance and potential loss of quality. Potential effects: poisoning, lack of efficacy, adverse reactions.

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Adrimax
Risk Level
High
Manufacturer
Zakłady Farmaceutyczne POLPHARMA S.A., Starogard Gdański
Batch Number
23371005A
EAN Code
05909991447304
Recall Date
08.11.2024
Category
Medicines & supplements
View official statement

Important Information

What You Should Know

Recommendations

Do not use products from the listed batches; check batch number and expiry date; return the product to the pharmacy or responsible entity; if taken and symptoms occur, consult a physician.

Actions Taken

The Chief Pharmaceutical Inspector withdrew the specified batches from nationwide circulation and prohibited their marketing; the decision was made immediately enforceable. The marketing authorization...

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: Localized turbidity of the Adrimax syrup solution detected in archived packages, indicating non-conforming appearance and potential loss of quality. Potential effects: poisoning, lack of efficacy, 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: 23371005A

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