Product Wiki · Recalls · EU Safety Gate (RAPEX)

My Family Doctor — recall A12/0037/19

EU Safety Gate (RAPEX) · Poland · 2019-01-11 · 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
A12/0037/19
Date of alert
2019-01-11
Country / jurisdiction
Poland
Risk level
Serious risk
Risk type
Chemical
Brand
MalPlay
Product category
Toys
Product type
Doctor play set
Reported risk: Materiał plastikowy jednego z elementów zestawu (tj. stetoskopu) zawiera ftalan bis(2-etyloheksylu) (DEHP) (zmierzona wartość: 20,2% wagowo) oraz ftalan dibutylu (DBP) (zmierzona wartość: 13,2% wagowo). Te ftalany mogą szkodzić zdrowiu dzieci, powodując możliwe uszkodzenie układu rozrodczego. Produkt nie jest zgodny z rozporządzeniem REACH.
Action taken by the authority
Type of economic operator taking notified measure
Importer
Category of measure
Withdrawal of the product from the market
Date of entry into force
13/11/2018
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): My Family Doctor

Risk Description (original English): The plastic material of one of the elements of the set (i.e.the stethoscope) contains 2-ethylhexyl phthalate (DEHP) (measured value: 20.2% by weight) and dibutyl phthalate (DBP) (measured value: 13.2% by weight).

Primary source: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/349464

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