SNIFFIT
SNIFFIT was recalled on 27 March 2026 under EU Safety Gate alert SR/00860/26. Health risk / other risk reported by Croatia. The product contains 23.
| Alert Number | SR/00860/26 |
| Category | Chemical products |
| Risk Type | Health risk / other |
| Notifying Country | Croatia |
| Country of Origin | Unknown |
| Published | 27 March 2026 |
Risk Description
The product contains 23.25% caffeine, taurine and menthol, which additionally stimulates blood circulation and increases the absorption of energetically active substances. Nasal application of this product causes rapid absorption, which, in addition to causing irritation of the mucous membrane, can lead to neurological effects and accelerated heart rate due to the risk of excessive intake, since the product does not contain a dispenser for uniform application. Excessive consumption may lead to risk of irritation, bleeding, and consequently infection and physiological changes in the nasal mucosa. The product does not comply with the GeneralProduct Safety Regulation.
Measures Taken
Type of economic operator to whom the measure(s) were ordered: ManufacturerCategory of measure(s): Withdrawal of the product from the marketDate of entry into force: 19/02/2026
Product Description
Energising white powder which is inhaled through the nose, 1 g. Product sold online, in particular via sniffit.life.
🏥 What Should You Do?
This recall involves a health risk / other hazard related to SNIFFIT.
About this risk
This product poses a health risk that does not fall neatly into a single category. It may involve multiple hazards or an unusual safety concern identified by authorities.
Recommended action
Stop using the product and follow any specific instructions from the recall notice. Contact the manufacturer or your national consumer protection authority for more details.
Who is at risk?
All consumers who have purchased this product.