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Recalled Medicines & supplements – Current GIS Alerts 2026

Found 713 recalled products in the Medicines & supplements category. Check batch numbers, shops, and hazard information.

Common hazards in this category

All recalled products

Paracetamol Aflofarm – recalled product

Paracetamol Aflofarm

HIGH 19.11.2024

Problem achieving a homogeneous suspension and residual sediment at the bottom of the bottle despite shaking; product information lacked a specified minimum shaking time. Potential effects: uneven dosing and reduced efficacy, risk of incorrect dosing.

Pulmopect – recalled product

Pulmopect

CRITICAL 14.11.2024

Non-uniform syrup consistency and presence of a gel-like floating substance not dissolving on shaking; out-of-specification result for microbiological purity. Potential effects: infections, risk of infection.

Pulmopect – recalled product

Pulmopect

CRITICAL 14.11.2024

non-homogeneous syrup consistency and presence of gel-like floating substance not dissolving upon shaking; OOS result for microbiological purity. Potential effects: infection, poisoning, risk of complications.

Enema – recalled product

Enema

MEDIUM 14.11.2024

Detected sediment as solid white flakes and turbidity of the solution, inconsistent with specification (product should be clear and free of mechanical impurities). Potential effects: irritation, infection risk, reduced efficacy.

Enema – recalled product

Enema

MEDIUM 14.11.2024

Sediment in bottles in the form of solid white particles and turbidity of the solution not meeting product specification. Potential effects: reduced efficacy, irritation, impaired product quality.

Adrimax – recalled product

Adrimax

HIGH 08.11.2024

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.

Pulmopect – recalled product

Pulmopect

MEDIUM 08.11.2024

Altered appearance: visible turbidity and jelly-like particles floating in the syrup, not dissolving after shaking; traces of leakage from the packaging. Potential effects: poisoning, lack of efficacy of treatment, adverse reactions.

Hydroxyzinum Hasco – recalled product

Hydroxyzinum Hasco

MEDIUM 05.11.2024

An increase of an unknown impurity was detected in the 'other single' parameter for hydroxyzine hydrochloride after a production pH-meter failure, resulting in non-compliance with quality specifications. Potential effects: unknown toxic effects, adverse reactions, reduced medicine quality.

Hydroxyzinum Hasco – recalled product

Hydroxyzinum Hasco

MEDIUM 05.11.2024

An increase of an unknown contaminant was detected in the 'other single' impurity parameter (hydroxyzine hydrochloride impurity) in batches 010624 and 020624. Potential effects: poisoning, reduced efficacy, adverse reactions.

BIOFLEKS % 0.9 Izotonik Sodyum Klorür çözeltisi Steril – recalled product

BIOFLEKS % 0.9 Izotonik Sodyum Klorür çözeltisi Steril

HIGH 18.10.2024

Observed presence of liquid between the primary container and outer film of unknown origin, indicating possible leakage of a parenteral container. Potential effects: infection, loss of sterility, unpredictable consequences upon administration.

Sugammadex Reig Jofre – recalled product

Sugammadex Reig Jofre

CRITICAL 03.10.2024

The presence of visible silicone particles in the product solution was found; the safety report indicates that potential risk to patients from injection of these particles cannot be excluded. Potential effects: vascular complications, inflammatory reactions, emboli, other injection-related complications.

Sugammadex Reig Jofre – recalled product

Sugammadex Reig Jofre

CRITICAL 03.10.2024

The submitted safety assessment report indicates that potential risk to patients from injection of visible silicone particles cannot be excluded. Potential effects: complications after injection, local or systemic reactions, health risk.

Euvax B – recalled product

Euvax B

CRITICAL 03.10.2024

Due to the occurrence of a threat to public health and a reported adverse post‑vaccination reaction potentially related to administration of this vaccine, the authority identified a real risk to patients’ health and life. Potential effects: serious adverse reactions, post‑vaccination complications, life‑threatening conditions.

Strepsils z miodem i cytryną – recalled product

Strepsils z miodem i cytryną

HIGH 24.09.2024

Contamination of the medicinal product with a substance of unknown origin and nature creates a real risk of unforeseeable medical consequences. Potential effects: poisoning, adverse reactions, lack of treatment efficacy.

Atofab – recalled product

Atofab

HIGH 20.09.2024

Out-of-specification results for atomoxetine content and non-uniform capsule mass, which may reduce product efficacy. Potential effects: reduced or absent therapeutic effect.

Atofab – recalled product

Atofab

HIGH 20.09.2024

Out-of-specification results for atomoxetine content and capsule mass uniformity (OOS) detected in reference tests. Potential effects: reduced efficacy of the medicine.

Atofab – recalled product

Atofab

MEDIUM 20.09.2024

Results out of specification (OOS) for atomoxetine content and non-uniformity of capsule mass in identified batches. Potential effects: reduced therapeutic efficacy.

Atofab – recalled product

Atofab

MEDIUM 20.09.2024

Out-of-specification results for atomoxetine content and non-uniform capsule mass caused by manufacturing defects and changed API particle properties. Potential effects: reduced efficacy of the medicine.

Corhydron 25 – recalled product

Corhydron 25

CRITICAL 18.09.2024

A quality defect was identified consisting of an out-of-specification result for free hydrocortisone content, with this exceedance expected to increase until the end of the shelf-life of batch 110021. Potential effects: reduced efficacy or unpredictable action of this life-saving emergency medicine.

Corhydron 25 – recalled product

Corhydron 25

CRITICAL 18.09.2024

An out-of-specification (OOS) result was found in stability testing for the free hydrocortisone content; further increase is expected until the end of shelf life of batch 110021, which may affect dissolution and the drug’s performance. Potential effects: reduced therapeutic efficacy or unpredictable effects of the injectable medicine.

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.