Product Wiki · Recalls · EU Safety Gate (RAPEX)

Adaptador de 2 vías — recall SR/00289/25

EU Safety Gate (RAPEX) · Spain · 2025-01-24 · 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/00289/25
Date of alert
2025-01-24
Country / jurisdiction
Spain
Risk level
Serious risk
Risk type
Electric shock
Brand
AIGOSTAR
Product category
Electrical appliances and equipment
Product type
Adaptor
Barcode (EAN/GTIN)
8433325192495
Reported risk: El adaptador se puede abrir con un destornillador común sin que quede totalmente inutilizable. El usuario podría manipularlo incorrectamente, tocar partes vivas accesibles y recibir una descarga eléctrica. El producto no cumple los requisitos de la Directiva de Baja Tensión.
Action taken by the authority
Type of economic operator to whom the measure were ordered
Distributor
Category of measure
Withdrawal of the product from the market
Date of entry into force
19/12/2024
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): Adaptador de 2 vías

Risk Description (original English): The adaptor can be opened using an ordinary screwdriver without leaving it totally unusable. The user could handle it incorrectly, touch accessible live parts and receive an electric shock.

Primary source: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10092745

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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.