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Recalled Medicines & supplements – Current GIS Alerts 2026

Found 685 recalled products in the Medicines & supplements category. Check batch numbers, shops, and hazard information.

Common hazards in this category

All recalled products

ADRENALIN OSEL (Adrenaline), 1 mg/1 mL IM/IV/SC Solution for Injection, Ampułka a 1 mg/ml, – recalled product

ADRENALIN OSEL (Adrenaline), 1 mg/1 mL IM/IV/SC Solution for Injection, Ampułka a 1 mg/ml,

CRITICAL 03.03.2023

Based on the collected data there is a risk to patients’ health and life due to the inability to use this life‑saving medicine and the possibility of administering a solution contaminated with glass. Potential effects: life‑threatening complications, tissue damage, acute systemic reactions.

ADRENALIN OSEL 1 mg/1 mL IM/IV/SC Solution for Injection – recalled product

ADRENALIN OSEL 1 mg/1 mL IM/IV/SC Solution for Injection

CRITICAL 23.02.2023

Breaking of the ampoule and inability to open the medicine normally, creating uncertainty whether glass fragments entered the interior and contaminated the solution, posing a threat to the patient’s health and life. Potential effects: life‑threatening complications after injection, tissue damage, lack of effective treatment.

Tirosint Sol – recalled product

Tirosint Sol

MEDIUM 21.02.2023

Due to the reduced active substance content found in these batches, a risk to patient health from decreased medicinal efficacy cannot be excluded. Potential effects: reduced treatment efficacy, disease worsening, complications related to insufficient therapy.

Tirosint Sol – recalled product

Tirosint Sol

MEDIUM 21.02.2023

Due to the reduced content of the active substance found in the above-mentioned batches, a risk to patient health arising from decreased effectiveness of the medicine cannot be ruled out. Potential effects: lack of treatment efficacy, worsening of disease symptoms.

Tirosint Sol – recalled product

Tirosint Sol

MEDIUM 21.02.2023

A reduced content of the active substance (levothyroxine) was found in five batches, with out-of-specification results and levels below the established limit, which may lead to decreased drug effectiveness and health risk for patients. Potential effects: reduced efficacy of hypothyroidism treatment, possible worsening of disease symptoms.

Tirosint Sol – recalled product

Tirosint Sol

MEDIUM 21.02.2023

Due to the reduced active substance content found in the above-mentioned batches, a risk to patient health from decreased efficacy of the medicine cannot be excluded. Potential effects: lack of treatment effectiveness, worsening disease control, possible complications of thyroid disorders.

Tirosint Sol – recalled product

Tirosint Sol

MEDIUM 21.02.2023

A decrease in active substance content below the limit and out-of-specification results for levothyroxine content were found, which may lead to reduced effectiveness of the medicine, and a risk to patient health cannot be excluded. Potential effects: reduced treatment effectiveness, worsening of disease symptoms, possible complications resulting from hypothyroidism.

Lorabex – recalled product

Lorabex

CRITICAL 16.02.2023

Suspected quality defect: out-of-specification (OOS) results for the parameters Lorazepam content and Lorazepam related substances, which may indicate an incorrect amount of active substance and impurities in the solution for injection. Potential effects: lack of treatment efficacy, excessive sedative effect, adverse reactions, complications.

Diprophos – recalled product

Diprophos

CRITICAL 31.01.2023

Possible occurrence of brown, metallic-looking particles in the suspension for injection, identified as stainless steel particles, which may cause local inflammatory conditions and hypersensitivity reactions at the injection site. Potential effects: local complications, inflammation, allergic reactions, post-procedural complications.

Diprophos – recalled product

Diprophos

CRITICAL 31.01.2023

A possible occurrence of brown particles with a metallic appearance, identified as stainless steel particles, was found in the suspension for injection. Potential effects: local inflammatory reactions, hypersensitivity, complications after injection of foreign bodies.

Bupicain – recalled product

Bupicain

CRITICAL 27.01.2023

The information leaflet for Bupicain contains incorrect data on the possibility of intravenous and intra-arterial administration of the medicine, which is associated with a threat to public health. Potential effects: incorrect administration, severe complications, life-threatening events.

Febrisan – recalled product

Febrisan

MEDIUM 26.01.2023

An out-of-specification result was found in stability testing: at 12 months the content limits for paracetamol and ascorbic acid were exceeded; it is uncertain whether the rest of the batch meets quality requirements for active substance content. Potential effects: reduced treatment efficacy or increased adverse effects.

Bupivacaine Hydrochloride in Dextrose Injection USP – recalled product

Bupivacaine Hydrochloride in Dextrose Injection USP

CRITICAL 10.01.2023

The defective ampoule may crumble, creating a risk of glass particles entering the anaesthetic solution administered to the patient and of being unable to use the medicine during surgery. Potential effects: tissue damage from glass, surgical complications, life-threatening risk, lack of effective anaesthesia.

Allergovit – recalled product

Allergovit

CRITICAL 10.01.2023

Because there is a risk of misleading medical staff and, consequently, the patient receiving too high a dose of the drug, which may result in a threat to patients’ life and health. Potential effects: life‑threatening reactions, severe allergic reactions, serious complications of therapy.

HERBS, Thyme and Coltsfoot – recalled product

HERBS, Thyme and Coltsfoot

CRITICAL 30.12.2022

Exceeded permissible level of pyrrolizidine alkaloids in the dietary supplement (batch 31722). Potential effects: liver damage, toxicity with prolonged consumption.

BOOSTERON HARDCORE TESTOSTERONE BOOSTER (120 capsules) – recalled product

BOOSTERON HARDCORE TESTOSTERONE BOOSTER (120 capsules)

HIGH 14.12.2022

Presence of undeclared substances: yohimbine and ibutamoren, which may cause serious adverse effects and hormonal disturbances. Potential effects: adverse reactions, heart rhythm disorders, hypertension, hormonal disturbances.

MMASTER Raspberry – pre-workout supplement – recalled product

MMASTER Raspberry – pre-workout supplement

HIGH 13.12.2022

Presence of undeclared yohimbine — an alkaloid from yohimbe bark banned in food. Potential effects: cardiovascular disturbances, hypertension, tachycardia, neuropsychiatric symptoms, risk of poisoning.

Allergovit – recalled product

Allergovit

CRITICAL 09.12.2022

Incorrect labeling of vials (concentration A-1000 TU/ml labeled as B-10,000 TU/ml) may mislead medical staff and result in administering too high a dose, endangering patients’ life and health. Potential effects: overdose, severe allergic reactions, serious complications, life-threatening conditions.

Bisoratio ASA – recalled product

Bisoratio ASA

MEDIUM 07.12.2022

An out-of-specification result was found in stability testing for the parameter bisoprolol fumarate related substances: another single impurity. The probability of adverse reactions after exposure to the product cannot be excluded. Potential effects: possible adverse reactions, including toxic symptoms or reduced treatment efficacy.

Rivanol 0,1% – recalled product

Rivanol 0,1%

CRITICAL 05.12.2022

An out-of-specification pH value was detected, which may affect the antibacterial activity of ethacridine. A defective series of glass bottles is the probable cause, and pH changes until expiry are unpredictable. Potential effects: lack of treatment efficacy, possible complications of infections.

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.