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Dinnesis Tofflor — recall A12/02577/24

EU Safety Gate (RAPEX) · Sweden · 2024-09-13 · 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
A12/02577/24
Date of alert
2024-09-13
Country / jurisdiction
Sweden
Risk level
Serious risk
Risk type
Chemical
Brand
Guanmei, Dinnesis
Product category
Clothing, textiles and fashion items
Product type
Children's slippers
Barcode (EAN/GTIN)
6972853820460
Reported risk: The plastic material of the shoes contains an excessive concentration of bis(2-ethylhexyl) phthalate (DEHP), dibutyl phthalate (DBP) and lead (measured values up to: 22 %, 24% and 0.25% by weight, respectively). These phthalates may harm the health of children by causing possible damage to their reproductive system. Lead is harmful to human health, accumulates in the body, can cause developmental neurotoxicity and may also affect breast-fed or unborn children.
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
Distributor
Category of measure
Removal of this product listing by the online marketplace
Date of entry into force
21/08/2024
Primary source: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10014352

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.