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Recalled Medicines & supplements – Current GIS Alerts 2026

Found 700 recalled products in the Medicines & supplements category. Check batch numbers, shops, and hazard information.

Common hazards in this category

All recalled products

IBUFEN DLA DZIECI FORTE O SMAKU TRUSKAWKOWYM – recalled product

IBUFEN DLA DZIECI FORTE O SMAKU TRUSKAWKOWYM

CRITICAL 10.09.2019

A quality defect consisting of an out-of-specification result for the ibuprofen content parameter in the medicinal product Ibufen for children Forte, strawberry flavour. Potential effects: lack of treatment efficacy or overdose leading to adverse reactions.

BENZACNE – recalled product

BENZACNE

MEDIUM 30.08.2019

A defective internal lacquer coating was found on the inner surface of the primary packaging (tube) used for packing the medicinal product, creating a substantiated potential risk to patients’ health or life. Potential effects: health complications, possible loss of medicine quality or safety.

ZOLAXA RAPID – recalled product

ZOLAXA RAPID

HIGH 29.08.2019

A quality defect was found: an out-of-specification result for the active substance content per tablet, which may mean an incorrect dose of the medicine for the patient. Potential effects: lack of treatment efficacy or increased adverse effects.

FOSIDAL O SMAKU MALINOWYM – recalled product

FOSIDAL O SMAKU MALINOWYM

CRITICAL 22.08.2019

A risk of use disproportionate to the therapeutic effect of the product containing fenspiride was identified, which may pose a real and highly probable threat to patients’ health or life. Potential effects: treatment complications, serious adverse reactions, threat to health or life.

EURESPAL – recalled product

EURESPAL

CRITICAL 22.08.2019

A risk of using the medicinal product Eurespal disproportionate to its therapeutic effect was identified, which may cause a significant threat to patients’ health or life. Potential effects: treatment complications, lack of efficacy, possible serious adverse reactions.

Elofen – recalled product

Elofen

CRITICAL 22.08.2019

Determination of a risk of use disproportionate to the therapeutic effect of the medicinal product Elofen, with a significant probability of harm to individuals and a real, highly probable threat to patients’ health or life. Potential effects: serious adverse reactions, complications, threat to health or life, lack of a favorable benefit‑risk balance.

FENSPOGAL – recalled product

FENSPOGAL

CRITICAL 22.08.2019

A risk of use disproportionate to the therapeutic effect was identified for products containing fenspiride, considered by PRAC and CMDh significant enough to recommend withdrawal of marketing authorizations. Potential effects: serious adverse reactions, risk to health or life, unacceptable safety profile.

PULNEO O SMAKU COLI – recalled product

PULNEO O SMAKU COLI

CRITICAL 22.08.2019

It was found that the benefit–risk ratio of medicinal products containing fenspiride is not favourable, and therefore withdrawal of marketing authorisations for these products was recommended. Potential effects: lack of adequate treatment efficacy, possible serious adverse reactions.

EURESPAL – recalled product

EURESPAL

CRITICAL 22.08.2019

A risk of use disproportionate to the therapeutic effect of the medicinal product Eurespal was identified, which may pose a direct threat to patients’ health or life. Potential effects: serious adverse reactions, threat to patients’ health or life.

EURESPAL – recalled product

EURESPAL

CRITICAL 22.08.2019

It was found that the benefit-risk balance of products containing fenspiride is unfavorable, meaning a risk of use disproportionate to the therapeutic effect and a potential threat to patients’ health or life. Potential effects: serious adverse reactions, life-threatening events, lack of safe therapy.

FOSIDAL O SMAKU POMARAŃCZOWYM – recalled product

FOSIDAL O SMAKU POMARAŃCZOWYM

CRITICAL 22.08.2019

It was found that the risk of using products containing fenspiride is disproportionate to their therapeutic effect, with a potential threat to patients’ health or life. Potential effects: serious adverse reactions, complications and life‑threatening events.

PULNEO – recalled product

PULNEO

CRITICAL 22.08.2019

It was determined that the benefit‑risk balance of medicinal products containing fenspiride, including Pulneo, is not favorable, which may pose a real threat to patients’ health or life. Potential effects: serious adverse reactions, threat to health or life.

EUREFIN – recalled product

EUREFIN

CRITICAL 22.08.2019

A risk of use of the medicinal product Eurefin disproportionate to its therapeutic effect was identified, meaning that the benefit–risk balance of medicines containing fenspiride is not favourable. Potential effects: serious adverse reactions, unacceptable safety profile, possible threat to patients’ health or life.

EURESPAL – recalled product

EURESPAL

CRITICAL 22.08.2019

A risk of use disproportionate to the therapeutic effect was identified for medicinal products containing fenspiride, meaning an unfavorable benefit–risk balance and potential health threat to patients. Potential effects: lack of treatment efficacy, complications from adverse reactions, risk to health or life.

PULNEO – recalled product

PULNEO

CRITICAL 22.08.2019

A use-related risk disproportionate to the therapeutic effect was identified for medicinal products containing fenspiride, with the benefit–risk balance considered unfavorable, which may pose a real threat to patients’ health or life. Potential effects: lack of treatment efficacy, complications, and risk to patient health or life.

EURESPAL – recalled product

EURESPAL

LOW 22.08.2019

No information in the text about a specific hazard, type of product defect, contamination, composition, or health risk for patients. Potential effects: impossible to assess risk, possible lack of efficacy or other undefined product-related issues.

CURATODERM – recalled product

CURATODERM

CRITICAL 20.08.2019

A quality defect was found consisting of out-of-specification results for the active substance content parameter during stability testing of the medicinal product Curatoderm. Potential effects: lack of treatment efficacy or abnormal product action.

BDS N – recalled product

BDS N

MEDIUM 20.08.2019

Out-of-specification results were found in archival samples regarding the content of budesonide-related substances, due to exceeded levels of impurities. Potential effects: reduced treatment effectiveness or adverse effects related to the presence of impurities.

THIOGAMMA – recalled product

THIOGAMMA

MEDIUM 13.08.2019

A quality defect was found consisting in non-compliance of the disintegration parameter with the specification, which may mean improper release of the active substance and failure to ensure the established quality of the medicinal product. Potential effects: lack of treatment efficacy or its reduction.

BDS N – recalled product

BDS N

CRITICAL 07.08.2019

Out-of-specification results were found in archival samples for the parameter of budesonide-related substances content, due to exceeded impurity levels. Potential effects: possible adverse effects, toxicity, or lack of expected drug efficacy.

What to do if you bought a recalled product?

If you have purchased any of the products listed above, stop using or consuming them immediately. You can return the product to the store where you bought it for a full refund. Keep the receipt if possible, but most stores will accept returns even without one.