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Medicines & supplements – Current GIS Alerts 2026

Found 735 alerts in the Medicines & supplements category. Check batch numbers, shops, and hazard information.

Common hazards in this category

All recalled products

Recalled product: Ciprofloxacin Kabi 400 mg/200 ml roztwór do infuzji

Ciprofloxacin Kabi 400 mg/200 ml roztwór do infuzji

GIF Critical 10.09.2021

It was found that Ciprofloxacin Kabi cartons contained bottles labeled Glucosum 5% Fresenius with the same batch number, indicating mix-up of infusion products and risk of administering the wrong medicine. Potential effects: lack of efficacy, infusion-related complications.

Recalled product: Arpixor

Arpixor

GIF Medium 27.08.2021

According to the MAH’s representative, there is a justified suspicion that the Arpixor 30 mg, 56 tablets batch does not meet quality requirements regarding appearance. Potential effects: lack of treatment effectiveness or unpredictable drug action.

Recalled product: Arpixor

Arpixor

GIF Medium 25.08.2021

The abnormal appearance of the tablets does not meet the product’s quality requirements and may lead to interruption of pharmacotherapy, which in turn may pose a risk to patients’ life or health. Potential effects: worsening of the disease, complications, risk to life or health.

Recalled product: Bisoratio ASA

Bisoratio ASA

GIF Medium 05.08.2021

Out-of-specification results were found for the parameter of related substances and total bisoprolol impurities during long-term 12‑month stability studies, which may affect the safety and efficacy of the medicine. Potential effects: reduced treatment effectiveness, adverse reactions, cardiovascular complications.

Recalled product: Apo-Simva 40

Apo-Simva 40

GIF High 26.07.2021

A confirmed out-of-specification result was found for cross-contamination of the medicinal product with acetylsalicylic acid and salicylic acid. Potential effects: risk of adverse effects, allergic reactions, bleeding or other complications due to unintended intake of additional active substances.

Recalled product: Ozzion

Ozzion

GIF High 09.07.2021

An out-of-specification result was found for the release parameter, meaning the drug may not release the active substance correctly and may not ensure effective therapy. Potential effects: lack of treatment efficacy, worsening of symptoms, complications.

Recalled product: Champix

Champix

GIF Critical 07.07.2021

The presence of N-nitroso-varenicline contamination was found in the bulk product batch, with the level of this impurity exceeding the limit set based on ICH M7 guidance. Potential effects: possible carcinogenic effect and other serious adverse reactions.

Recalled product: Amiodaron Hameln

Amiodaron Hameln

GIF Critical 25.06.2021

Particles were detected in some ampoules of the concentrate for solution for injection or infusion, which according to the specification should be clear, light yellow and free from visible particles. Potential effects: risk of emboli, local reactions, circulatory complications or other serious complications during intravenous administration.

Recalled product: Flutixon Neb

Flutixon Neb

GIF Medium 14.06.2021

An out-of-specification result was found for the content of related substances in the product batches, which constitutes a quality defect and a potential risk to patients' health. Potential effects: possible adverse reactions, altered treatment efficacy, unpredictable bodily responses.

Recalled product: Flutixon Neb

Flutixon Neb

GIF Medium 14.06.2021

An out-of-specification result was found regarding the content of related substances in the medicinal product Flutixon Neb. Potential effects: reduced treatment efficacy or unpredictable adverse reactions.

Recalled product: Petroleum D4

Petroleum D4

GIF Low 11.05.2021

Incorrect expiry date labelling was found: the packaging shows 02.2022, while the correct date is 09.2022. Potential effects: possible premature disposal of the medicine or doubts about its validity.

Recalled product: Lignocain 2%

Lignocain 2%

GIF Critical 02.04.2021

A foreign body was identified in an individual immediate container, i.e. in a 20 ml vial of the Lignocain 2% solution for injection. Potential effects: infection, inflammatory reactions, local and systemic complications, including life-threatening conditions.

Recalled product: Febrisan

Febrisan

GIF Medium 26.03.2021

A quality defect was found consisting of micro-damages in the structure of the primary packaging foil, which may lead to loss of tightness and deterioration of the medicine’s quality. Potencjalne skutki: reduced treatment efficacy or adverse reactions.

Recalled product: Silimax

Silimax

GIF High 11.03.2021

Irregularities in batch number labelling were found: containers with batch number 05022020 were packed into cartons incorrectly marked as 02022020, preventing unambiguous identification of the product batch. Potential effects: risk of mix-ups and hindered recall in case of safety issues.

Recalled product: Formoterol Easyhaler

Formoterol Easyhaler

GIF High 03.03.2021

A quality defect of the Easyhaler inhaler was found in the reservoir chamber containing the inhalation powder; the impact of this defect on the quality and correct dosing of the medicinal products cannot be excluded, creating a potential risk to patients’ health or life. Potential effects: lack of efficacy, disease exacerbation, respiratory complications.

Recalled product: Bufomix Easyhaler

Bufomix Easyhaler

GIF High 03.03.2021

A quality defect was identified in the Easyhaler inhaler, in the reservoir chamber containing the inhalation powder; as a defect of the immediate packaging it may affect the medicinal product quality and dose delivery. Potential effects: lack of treatment efficacy, possible worsening of disease symptoms.

Recalled product: Nitroxolin forte

Nitroxolin forte

GIF High 25.02.2021

An impurity 5,7-Dinitro-8-quinolinol (DNC) was identified in the active substance and classified as a mutagenic impurity, whose content should be lower than currently approved limits. Potential effects: increased risk of DNA damage, cancer and other complications.

Recalled product: Hemkortin-HC

Hemkortin-HC

GIF High 18.02.2021

Incorrect strength of the medicinal product was found on the immediate (tube) packaging, which may mislead patients or medical staff about the dose being used. Potential effects: improper dosing, lack of therapeutic efficacy or increased adverse reactions.

Recalled product: Biodacyna

Biodacyna

GIF Critical 27.01.2021

A quality defect was found: an out‑of‑specification result for the colour parameter in a parenterally administered medicinal product, which entails a potential risk to patients’ health or life. Potential effects: complications after intravenous or intramuscular administration, lack of treatment safety.

Recalled product: Tlen medyczny Air Products

Tlen medyczny Air Products

GIF Medium 28.12.2020

An unusual odour was detected in one of the cylinders from the batch of the medicinal product Medical oxygen Air Products, indicating a quality defect of the medical gas and a potential health risk to patients when used. Potential effects: irritation of the respiratory tract, unspecified adverse reactions, lack of safety of oxygen therapy.

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.