# Commission Implementing Decision (EU) 2019/417 of 8 November 2018 laying down guidelines for the management of the European Union Rapid Information System ‘RAPEX’ established under Article 12 of Directive 2001/95/EC on general product safety and its notification system (notified under document C(2018) 7334), Division 4.2: Categories of measures

Extent: E+W+S+N.I.

Article 8(1)(b) to (f) of the GPSD provides a list of the different categories of measures that are notifiable under RAPEX when the conditions for notification are fulfilled, including the following measures:
(a) marking a product with appropriate warnings on the risk(s) it may present;
(b) making the marketing of a product subject to prior conditions;
(c) warning consumers and end-users of the risks that could be posed by a product;
(d) temporary ban on the supply, offer to supply and display of a product;
(e) ban on the marketing of a product and any accompanying measures, i.e. measures required to ensure compliance with the ban;
(f) withdrawal of a product from the market;
(g) recall of a product from consumers;
(h) destruction of a withdrawn or recalled product.
For the purpose of RAPEX, the term ‘withdrawal’ is used exclusively for measures aimed at preventing the distribution, display and offer of a product posing a risk to consumers or other end-users, while the term ‘recall’ is used only for measures aimed at achieving the return of such a product that has already been made available to consumers or other end-users by a producer or distributor.

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Source: https://www.legislation.gov.uk/eudn/2019/417/annex/division/1/part/I/division/4/division/4.2 (the official version)
Page: https://openlegislation.uk/eu-decision-2019-417/annex/division-1/part-I/division-4/division-4.2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.