Product Wiki · Recalls · EU Safety Gate (RAPEX)

ULTRA EDITION — recall SR/01499/26

EU Safety Gate (RAPEX) · Czechia · 2026-05-29 · Serious risk

Machine-translated with AI — the facts come from the issuing authority’s own notice (linked on this page); this language version was translated automatically by an AI model and is not reviewed. The original-language notice is authoritative. How we use AI →
Agency
EU Safety Gate (RAPEX)
Recall identifier
SR/01499/26
Date of alert
2026-05-29
Country / jurisdiction
Czechia
Risk level
Serious risk
Risk type
Chemical
Brand
BLUE FOR MEN
Product category
Cosmetics
Product type
Perfume
Barcode (EAN/GTIN)
8439627600348
🔴 Serious hazard — Reported risk: Výrobek obsahuje limonen, citronellol, citral, alpha-isomethyl lonone a benzyl salicylát, ale jejich přítomnost není uvedena v seznamu složek. Spotřebitelé si nejsou vědomi jejich přítomnosti a mohou utrpět alergické reakce nebo senzibilizaci kůže. Výrobek nesplňuje požadavky nařízení o kosmetických výrobcích.
Action taken by the authority
Type of economic operator to whom the measure were ordered
Retailer
Category of measure
Withdrawal of the product from the market
Date of entry into force
12/05/2026
Machine translation. This page was translated automatically from the English record we hold of the issuing authority’s notice. The English original is shown below and the authority’s own notice is linked above — both take precedence over this translation.

Product Name (original English): ULTRA EDITION

Risk Description (original English): The product contains limonene, citronellol, citral, alpha-isomethyl lonone and benzyl salicylate, but the presence is not indicated in the list of ingredients. Consumers are not aware of their presence, and may suffer allergic reactions or skin sensitisation.

Primary source: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10098976

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.