Product Wiki · Recalls · EU Safety Gate (RAPEX)

Fauteuil licorne — safety alert INFO/00001/24

EU Safety Gate (RAPEX) · France · 2024-01-05 · Other types of alerts

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
INFO/00001/24
Date of alert
2024-01-05
Country / jurisdiction
France
Authority classification
Other types of alerts
Risk type
Choking
Brand
Maisons du Monde
Product category
Furniture
Product type
Armchair for children
Reported risk: Le fauteuil contient des trous et le rembourrage est donc accessible. Le matériau de rembourrage fibreux du fauteuil est facilement accessible en raison de trous. Un jeune enfant peut mettre le matériau de rembourrage à la bouche et s'étouffer. Ce produit n'est pas conforme aux exigences de la directive relative à la sécurité générale des produits
Action taken by the authority
Type of economic operator taking notified measure
Manufacturer
Category of measure
Recall of the product from end users
Date of entry into force
20/11/2023
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): Fauteuil licorne

Risk Description (original English): The armchair contains holes and the padding is thus accessible. The fibrous stuffing material of the armchair is easily accessible due to holes. A small child may put the filling material in the mouth and choke.

Primary source: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10011340

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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.