| *First language: |
| Second language: |
| A.Notifying Member State: |
- 1)Country:
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- 2)Competent authority – contact details:
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- *3)Date of notification (DD/MM/YYYY):
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- *4)Reference
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| B.Notified Member State or Member States: |
- *1)Country/countries:
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- 2)Competent authority/authorities – contact details:
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| C.Product: |
- *1)Category of product:
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- *2)Product/trade name:
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- *3)Country of origin:
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- 4)Description of the product (packaging size and form, etc.) – please attach copied or scanned seal or label:
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- 5)Identification of the lot (e.g. lot number, delivery number, delivery date, etc.):
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- 6)Other information:
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| D.Traceability: |
| Please describe in detail the complete supply chain: |
- 1)Producer – contact details – competent authority or, where appropriate, the control authority or control body:
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- 2)Processor/seller in the country of origin – contact details – competent authority or, where appropriate, the control authority or control body:
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- 3)Importer in the notifying country – contact details – competent authority or, where appropriate, the control authority or control body:
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- 4)Wholesaler – contact details – competent authority or, where appropriate, the control authority or control body:
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- 5)Retailer or other operator in the notifying country, where the non-compliance has been detected – contact details – competent authority or, where appropriate, the control authority or control body:
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| Authority (ies): |
| Other actors: |
| E.Non-compliance, suspicion of non-compliance, other problem raised: |
- *1)Nature of the non-compliance/suspicion of non-compliance/other problem raised.
Which non-compliance/suspicion of non-compliance/other problem raised has been identified?: |
| *In what aspect does it represent a non-compliance/suspicion of non-compliance/other problem raised with Regulation (EU) 2018/848 of the European Parliament and of the CouncilRegulation (EU) 2018/848 of the European Parliament and of the Council of 30 May 2018 on organic production and labelling of organic products and repealing Council Regulation (EC) No 834/2007 (OJ L 150, 14.6.2018, p. 1).?: |
- 2)Context of the detection of the non-compliance/suspicion of non-compliance/other problem raised – please attach a copy of invoice or other supporting documents:
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| Date of the detection of the non-compliance/suspicion of non-compliance/other problem raised (DD/MM/YYYY): |
| Place of the detection of the non-compliance/suspicion of non-compliance/other problem raised: |
- 3)Analysis of the samples/tests (if any) – please attach a copy of analysis report:
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| Date of sampling/testing (DD/MM/YYYY): |
| Place of sampling/testing: |
| Date of the analysis – report (DD/MM/YYYY): |
| Details (name of the laboratory, methods used, results): |
| Name of the substances found: |
| Level of the residues detected: |
| Is the level above the threshold allowed in food (or feed) in general?: |
| Is the level for labeling of GMO-contents overshot?: |
| F.Market influence: |
- 1)Has the product been withdrawn from the market, blocked or marketed?:
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- 2)Which actors have been already informed?:
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- 3)Are other Member States affected? If so, which Member States?:
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| G.Measures taken: |
- 1)Have any voluntary measures been taken (on the product/operator/market)?:
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- 2)Have any compulsory measures been taken?:
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- 3)What is the scope of the measures (national, regional, exports, etc.)?:
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- 4)Date of entry into force: (DD/MM/YYYY):
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- 5)Duration (in months):
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- 6)Justification/legal basis of the measures:
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- 7)Which competent authority or, where appropriate, control authority or control body has adopted the measures?:
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| H.Other information/Evaluation: |
| I.Annexes: |
| Copied or scanned documentation of the product (seal, label, etc.). Copy of invoice, documentary account or document of transport or delivery order. Analysis report and/or any other relevant documents: |