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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: BUDIXON NEB

BUDIXON NEB

GIF Medium 01.08.2019

Exceeding the specification limit for the parameter of budesonide-related substances was found for batch 060218 and a probability of exceeding the limit for other in-date batches. Potential effects: lack of treatment efficacy or unpredictable adverse reactions.

Recalled product: PŁYN BUROWA

PŁYN BUROWA

GIF Medium 24.07.2019

Out-of-specification results were found in the ongoing stability program for parameters: appearance and purity — sulfate content, meaning the medicinal product does not meet established quality requirements. Potential effects: lack of therapeutic efficacy or unforeseen adverse reactions.

Recalled product: POLYVACCINUM MITE

POLYVACCINUM MITE

GIF Critical 17.07.2019

In one bottle of the medicinal product batch a solid body floating on the surface of the suspension was found, which poses a potential risk to patients' health. Potential effects: complications after administration, irritation, inflammatory reaction, lack of therapeutic efficacy.

Recalled product: BDS N

BDS N

GIF Medium 17.07.2019

Out-of-specification results were found for the content of related substances of budesonide, due to exceeded impurity levels. Potential effects: lack of treatment efficacy or adverse reactions caused by impurities.

Recalled product: ROZAPROST MONO

ROZAPROST MONO

GIF Low 15.07.2019

No information in the text about the type of hazard, contamination, quality defect or safety issue concerning a specific medicinal product or batch. Potential effects: impossible to assess risk, need to exercise caution until full data are obtained.

Recalled product: ROZAPROST MONO

ROZAPROST MONO

GIF Low 15.07.2019

No information in the text about any specific hazard to the quality, safety, or efficacy of any medicinal product. Potential effects: no effects can be determined based on the available information.

Recalled product: BENODIL

BENODIL

GIF Medium 10.07.2019

A risk was identified that the finished product may not meet specification requirements regarding the level of related substances, indicating a possible quality defect. Potential effects: possible lack of efficacy or unpredictable adverse reactions.

Recalled product: BENODIL

BENODIL

GIF Critical 10.07.2019

Risk of not meeting finished product specification with respect to the parameter of related substances content, which may indicate a quality defect of the medicinal product. Potential effects: lack of efficacy or unpredictable adverse reactions.

Recalled product: BUDIXON NEB

BUDIXON NEB

GIF Medium 04.07.2019

Exceeding the specification limit for the parameter of budesonide-related substances content was found, meaning the product does not meet established quality requirements. Potential effects: possible lack of treatment efficacy or adverse reactions.

Recalled product: BDS N

BDS N

GIF Critical 01.07.2019

The specification limit for the parameter "content of related substances" was exceeded due to increased impurity content, constituting a quality defect of the medicinal product and a potential risk to patients' health. Potential effects: poisoning, adverse reactions, lack of therapeutic efficacy.

Recalled product: BDS N

BDS N

GIF Critical 01.07.2019

It was confirmed that the specification limit for the parameter 'content of related substances' was exceeded, due to an increased level of impurities. Potential effects: possible adverse reactions, toxicity, lack of therapeutic efficacy.

Recalled product: ASANIX

ASANIX

GIF High 28.06.2019

A quality defect was found: in the ongoing stability testing program an out-of-specification result was obtained for the parameter of active substance release from the tablet, meaning the drug may not release the correct amount of active ingredient. Potential effects: lack of treatment efficacy or unpredictable drug action.

Recalled product: BENODIL

BENODIL

GIF Medium 27.06.2019

It was found that the specification limit for the related substances content parameter was exceeded, meaning the product does not meet established quality requirements. Potential effects: possible lack of efficacy, unpredictable adverse reactions.

Recalled product: 3% ROZTWÓR KWASU BOROWEGO

3% ROZTWÓR KWASU BOROWEGO

GIF Medium 19.06.2019

A quality defect was found: boric acid content 0.3% instead of the required 2.8–3.2% and a non‑compliant form of the raw material, which may lead to compounding magistral medicines with incorrect strength. Potential effects: lack of treatment efficacy, possible disease complications.

Recalled product: 3% ROZTWÓR KWASU BOROWEGO

3% ROZTWÓR KWASU BOROWEGO

GIF Critical 19.06.2019

A quality defect was found: boric acid content is 0.3% instead of 2.8%-3.2% and the form is non-compliant, which may lead to compounded medicines with incorrect strength and efficacy. Potential effects: lack of therapeutic efficacy, possible disease complications.

Recalled product: 3% ROZTWÓR KWASU BOROWEGO

3% ROZTWÓR KWASU BOROWEGO

GIF High 19.06.2019

A quality defect was found: too low boric acid content (should be 2.8%–3.2%, actual 0.3%) and non‑compliant form, which may lead to preparation of compounded medicines with incorrect strength and effectiveness. Potential effects: lack of drug efficacy, risk of therapy complications.

Recalled product: CALCIUM POLFARMEX (O SMAKU TRUSKAWKOWYM)

CALCIUM POLFARMEX (O SMAKU TRUSKAWKOWYM)

GIF Medium 13.06.2019

A quality defect of the medicinal product was found in the form of an improper smell of the syrup, which may indicate irregularities in the composition or stability of the product. Potential effects: lack of efficacy, possible irritation or other adverse reactions.

Recalled product: ARTHRYL

ARTHRYL

GIF Critical 07.06.2019

The defect consists in the use of incorrect serialization data, resulting in incorrect identification of the medicinal product and failure to meet requirements for verification of authenticity and identification of the pack. Potential effects: possible use of an inappropriate or falsified drug, lack of treatment efficacy, treatment complications.

Recalled product: VALZEK

VALZEK

GIF Critical 06.06.2019

Presence of N-nitrosodimethylamine (NDMA) contamination above the acceptable limit was found in the active substance Valsartan, which may pose a threat to patients' health and life. Potential effects: poisoning, carcinogenic effects, health complications with long-term use.

Recalled product: VALZEK

VALZEK

GIF Critical 06.06.2019

This risk may be caused by the presence of N-nitrosodimethylamine (NDMA) contamination in the active substance contained in the medicinal product, which may affect human health and life. Potential effects: possible carcinogenic effects and other serious health disorders with long-term exposure.

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.