Article 43 › 5

The information referred to in paragraph 4 shall include all available details, in particular the data necessary for the identification of the non-compliant product within the scope of this Regulation, the origin of that product, the nature of the non-compliance alleged and the risk involved, the nature and duration of the national measures taken and the arguments put forward by the relevant economic operator. In particular, the market surveillance authorities shall indicate whether the non-compliance is due to any of the following: (a) the failure of the product to meet the requirements relating to the essential health and safety requirements set out in Annex III; (b) shortcomings in the harmonised standards referred to in Article 20(1); (c) shortcomings in the common specifications referred to in Article 20(6).

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Source: EUR-Lex CELLAR · retrieved 2026-08-26