Product Wiki · Recalls · EU Safety Gate (RAPEX)

Ma petite lumière — recall SR/01397/25

EU Safety Gate (RAPEX) · France · 2025-04-11 · Serious risk

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked on this page. No AI-generated text appears on this page. How we use AI →
Agency
EU Safety Gate (RAPEX)
Recall identifier
SR/01397/25
Date of alert
2025-04-11
Country / jurisdiction
France
Risk level
Serious risk
Risk type
Chemical, Choking
Brand
ROLDAN
Product category
Toys
Product type
Toy unicorn
Barcode (EAN/GTIN)
3700281180503
Reported risk: The product has small parts which may easily detach (horn and ears). Moreover, the battery compartment can be easily opened, leaving the button batteries accessible. A child may put them in the mouth and swallow them, which could cause damage to the child’s gastrointestinal tract and/or choking. The product does not comply with the requirements of the Toy Safety Directive nor with European standard EN 62115.
What to do

Check whether your product matches this notice (name, batch, dates). If it does, stop using it and follow the instructions in the official notice — refund, return, repair or disposal are set by the issuing authority and the business, and they differ per recall. Official notice from EU Safety Gate (RAPEX) →

Action taken by the authority
Type of economic operator taking notified measure
Manufacturer
Category of measure
Withdrawal of the product from the market
Date of entry into force
11/03/2025
Primary source: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10093897

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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.