Product Wiki · Recalls · EU Safety Gate (RAPEX)

Blue Edition — recall A12/02167/24

EU Safety Gate (RAPEX) · Hungary · 2024-08-16 · 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
A12/02167/24
Date of alert
2024-08-16
Country / jurisdiction
Hungary
Risk level
Serious risk
Risk type
Chemical
Brand
Elina med
Product category
Cosmetics
Product type
Eau de toilette
Barcode (EAN/GTIN)
4326470457905
Reported risk: Az összetevők listája szerint a termék 2-(4-terc-butilbenzil)propionaldehidet (BMHCA) tartalmaz, amely kozmetikai termékekben tiltott. A BMHCA károsíthatja a reproduktív rendszert, károsíthatja a születendő gyermek egészségét, és bőrszenzibilizációt okozhat. A termék nem felel meg a kozmetikai termékekről szóló rendeletnek.
Action taken by the authority
Type of economic operator to whom the measure were ordered
Distributor
Category of measure
Recall of the product from end users
Date of entry into force
28/11/2023
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): Blue Edition

Risk Description (original English): According to the list of ingredients the product contains 2-(4-tert- butylbenzyl) propionaldehyde (BMHCA), which is forbidden in cosmetic products. BMHCA may harm the reproductive system, may harm the health of the unborn child and may cause skin sensitisation.

Primary source: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10014041

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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.