oAlert.pl

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: Tetmodis

Tetmodis

GIF Medium 26.02.2020

Out-of-specification results were found for active substance content in batch T1702PL of Tetmodis (Tetrabenazine), which may mean an inappropriate dose for the patient. Potential effects: lack of efficacy or increased adverse effects.

Recalled product: Sulfarinol

Sulfarinol

GIF High 21.02.2020

Out-of-specification results were found in archival samples of Sulfarinol batches for the parameter “naphazoline nitrate contamination – other single impurity”, indicating a quality defect of the product. Potential effects: reduced treatment efficacy and possible adverse reactions of unpredictable intensity.

Recalled product: Flegafortan

Flegafortan

GIF High 14.02.2020

It was found that the patient leaflet regarding recommended dosing was inconsistent with the Summary of Product Characteristics, which could lead to incorrect use of the product and overdose manifested by unintended increased volume of bronchial secretions. Potential effects: overdose, increased bronchial secretion, respiratory complications.

Recalled product: Mitomycin Accord

Mitomycin Accord

GIF Critical 12.02.2020

A quality defect was found consisting in the inability to dissolve the powder, which may prevent preparation of a correct injection/infusion solution and result in failure to administer the proper drug dose. Potential effects: lack of treatment efficacy, complications of oncological therapy.

Recalled product: Flegafortan

Flegafortan

GIF High 27.01.2020

The patient leaflet regarding recommended dosing was inconsistent with the approved Summary of Product Characteristics, which could lead to incorrect use and overdose manifested by increased volume of bronchial secretions. Potential effects: overdose, worsening cough and adverse drug reactions.

Recalled product: Sulfarinol

Sulfarinol

GIF Critical 13.01.2020

The tested retention samples showed out-of-specification results for the parameter “naphazoline nitrate contamination – other single impurity”, which may indicate the presence of an undesirable chemical compound in the product. Potential effects: possible adverse effects, irritation, lack of efficacy or other unpredictable reactions.

Recalled product: Espumisan 100 mg/ml

Espumisan 100 mg/ml

GIF High 10.01.2020

In several packs of the product, information leaflets for the medicinal product Zentel were detected instead of the correct Espumisan leaflet. Potential effects: incorrect use of the medicine, risk of improper dosing or lack of treatment efficacy.

Recalled product: Lecalpin

Lecalpin

GIF High 03.01.2020

The defect was reported due to the detection of Lecalpin 10 mg blisters, batch 268018, inside outer cartons intended for Lecalpin 20 mg. Potential effects: possible intake of an incorrect dose and reduced treatment efficacy.

Recalled product: Kalium effervescens bezcukrowy

Kalium effervescens bezcukrowy

GIF High 16.12.2019

Lack of a unique identifier and an anti-tampering device on the packaging of prescription-only products, which could hinder verification of authenticity and detection of package tampering. Potential effects: risk of falsified medicine or interference with the packaging, possible lack of efficacy or adverse effects.

Recalled product: Spasmolina

Spasmolina

GIF High 16.12.2019

The non-compliance consisted in not placing on the packaging of prescription medicinal products the safety features: a unique identifier and an anti-tampering device. Potential effects: falsification of the medicine, misidentification, risk of lack of appropriate treatment.

Recalled product: Riflux

Riflux

GIF Critical 05.12.2019

Contamination of the active substance Ranitidine with N-nitrosodimethylamine (NDMA) was detected, constituting a quality defect and a potential risk to patients’ health. Potential effects: possible toxic and carcinogenic effects during long-term use.

Recalled product: Debridat

Debridat

GIF Critical 22.11.2019

A potential quality defect was reported due to the risk of a foreign body being present in the product, which may pose a real and direct risk to patients’ health or life. Potential effects: complications, tissue damage, life-threatening events.

Recalled product: Debridat

Debridat

GIF Critical 22.11.2019

Risk of a potential quality defect consisting in the presence of a foreign body in the product. Potential effects: mechanical injuries, gastrointestinal complications, risk to health or life.

Recalled product: Debridat

Debridat

GIF Critical 22.11.2019

Risk of the presence of a foreign body in the medicinal product, possibly due to a potential quality defect. Potential effects: mechanical damage to the gastrointestinal tract, complications, need for medical intervention.

Recalled product: Debridat

Debridat

GIF Critical 22.11.2019

Risk of presence of a foreign body in the medicinal product Debridat (Trimebutinum), 7.87 mg/g, granules for oral suspension. Potential effects: mechanical damage, complications, irritation of the gastrointestinal tract.

Recalled product: Debridat

Debridat

GIF Critical 22.11.2019

Risk of the presence of a foreign body in the medicinal product Debridat (Trimebutinum), 7.87 mg/g, granules for oral suspension, which may cause gastrointestinal damage or other mechanical complications during use. Potential effects: mechanical injuries, complications, risk to health or life.

Recalled product: Debridat

Debridat

GIF Critical 22.11.2019

Risk of a quality defect in the medicinal product Debridat, 7.87 mg/g, granules for oral suspension, due to the risk of the presence of a foreign body in the product. Potential effects: gastrointestinal injuries, complications, possible threat to the patient’s health or life.

Recalled product: Debridat

Debridat

GIF Critical 20.11.2019

Risk of presence of a foreign body in the medicinal product Debridat (Trimebutinum), 7.87 mg/g, granules for oral suspension, which may expose the patient to mechanical damage of the gastrointestinal tract or other complications during use. Potential effects: injuries, complications, health risk.

Recalled product: Apra-swift

Apra-swift

GIF High 20.11.2019

A printing inconsistency in the dose on one side of the outer packaging was found (15 mg stated incorrectly, it should be 30 mg). Potential effects: improper dosing, lack of treatment efficacy or adverse effects.

Recalled product: Raniberl Max

Raniberl Max

GIF High 08.11.2019

Contamination of the active substance ranitidine with N-nitrosodimethylamine (NDMA) was detected, causing the batches to be deemed non-compliant with quality requirements and potentially hazardous to patients’ health or life. Potential effects: carcinogenic action, organ damage, general poisoning.

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.