# 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 3.4.6.2: Objectives of the follow-up activities

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

On receipt of a notification, a Member State examines the information provided in the notification and takes appropriate action in order to:
(a) establish whether the product was marketed on its territory;
(b) assess what preventive or restrictive measures should be taken with regard to the notified product found on its market, taking into account the measures taken by the notifying Member State and any special circumstances that could justify different types of measures or no action being taken;
(c) perform additional risk assessment and testing of the notified product, if necessary;
(d) collect any additional information that may be relevant for other Member States (e.g. information on distribution channels of the notified product in other Member States).

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Source: https://www.legislation.gov.uk/eudn/2019/417/annex/division/1/part/II/division/3/division/3.4/division/3.4.6/division/3.4.6.2 (the official version)
Page: https://openlegislation.uk/eu-decision-2019-417/annex/division-1/part-II/division-3/division-3.4/division-3.4.6/division-3.4.6.2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.