reg 56 Enforcement action in respect of products which are not in conformity and which present a risk
(1) Where, in the course of the evaluation referred to in regulation 55 , the market surveillance authority finds that the product is not in conformity with Part 2, it must, without delay, require a relevant economic operator to— (a) take appropriate corrective action to bring the product into conformity with those requirements within a prescribed period, (b) withdraw the product within a prescribed period, or (c) recall the product within a prescribed period. (2) The market surveillance authority must inform the approved body which carried out the conformity assessment procedure in respect of the product of— (a) the respect in which the product is not in conformity with Part 2, and (b) the actions which the market surveillance authority is requiring the relevant economic operator to take. (3) Where the market surveillance authority considers that the lack of conformity referred to in paragraph (1) is not restricted to Great Britain, it must notify the Secretary of State of— (a) the results of the evaluation, and (b) the actions which it has required the economic operator to take. (4) Where the Secretary of State receives a notice under paragraph (3), or otherwise considers that the lack of conformity referred to in paragraph (1) is not restricted to Great Britain, the Secretary of State must inform the Health and Safety Executive for Northern Ireland of— (a) the results of the evaluation, and (b) the actions which the market surveillance authority has required the economic operator to take. (5) Where the relevant economic operator does not take adequate corrective action within the prescribed period, the market surveillance authority must take appropriate measures to— (a) prohibit or restrict the product being made available on the market in Great Britain, (b) withdraw the product from the market in Great Britain, or (c) recall the product. (6) Where the market surveillance authority takes measures under paragraph (5), it must notify the Secretary of State of those measures without delay. (7) Where the Secretary of State receives a notice under paragraph (6), the Secretary of State must notify the Health and Safety Executive for Northern Ireland of those measures without delay. (8) The notices in paragraphs (6) and (7) must include details about the product and, in particular— (a) the data necessary for the identification of the product which is not in conformity with Part 2; (b) the origin of the product; (c) the nature of the lack of conformity alleged and the risk involved; (d) the nature and duration of the measures taken; (e) the arguments put forward by the relevant economic operator; (f) whether the lack of conformity is due to either of the following— (i) failure of the product to meet requirements relating to a risk; (ii) shortcomings in the designated standards referred to in regulation 38 (presumption of conformity) conferring a presumption of conformity. (9) In this regulation, “prescribed period” means a period which is— (a) prescribed by the market surveillance authority; (b) reasonable and commensurate with the nature of the risk presented by the product.