# 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 2: Fields and information included in follow-up notifications

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

Fields that will be published on the web are shaded.
* Indicates a mandatory field
Section 1: General information
Case number
Validated notification type
Notifying country
Creation date
Validation/distribution date
Submission number
Follow up notification number
Reacting country
Full contact details of the notifying authority
Validated notification product category
Notified product
Notified name
Product (what the product is)
Name (on the product or the packaging)
Brand (on the product or the packaging)
Type/number of model
Batch number/Bar code (or other information to identify which products are affected)
Photos (products, packaging and label)
Section 2: Type of follow-up notification
Product found *
Total number of items found (if known) *
Measures adopted / Measures not adopted
Type of measures adopted *
If Voluntary:
Type of economic operator taking notified measure(s) *
Name of economic operator taking notified measure(s) *
If Compulsory:
Name of authority ordering the notified measure(s) *
Type of economic operator to whom the measure(s) were ordered *
Category of measures *
Date of entry into force *
Duration *
Scope *
Adopted measures
URL link to company recall page (if available):
Different risk assessment *
Risk category *
Summary of the test results (description of technical defects) *
Indication of legal provisions and standards (with clauses) against which the product was tested *
Different risk assessment *
Information on known incidents and accidents *
Attachments (certificates, test report and risk assessment …)
Additional information *
Complementary information on distribution channels and/or product's origin
Complementary information on the risk assessment
Other complementary information
Section 3: Confidentiality
Is the follow-up confidential? *
Scope of confidentiality
Justification
Annexes
Photos (product, packaging and label)
Test reports and risk assessments
Certificates
Adopted measures

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Source: https://www.legislation.gov.uk/eudn/2019/417/annex/division/1/part/III/division/2 (the official version)
Page: https://openlegislation.uk/eu-decision-2019-417/annex/division-1/part-III/division-2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.