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WTO notification · SPS

European UnionCorrected since it was notified

Meat and edible meat offal; Cereals – European Union

Official title

Draft Commission Regulation amending Annexes II, III and V to Regulation (EC) No 396/2005 of the European Parliament and of the Council as regards maximum residue levels for azocyclotin, chlorfenapyr, cyhexatin, dicofol, endosulfan, fenarimol, fenpropathrin and profenofos in or on certain products (Text with EEA relevance)

The European Union issued a correction on 10 July 2026 to the earlier SPS notification G/SPS/N/EU/959. The measure was first notified on 26 June 2026. The comment period closed on 25 August 2026.

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Source: WTO ePing (opens in a new tab). Summaries by Expodite, which is independent of the WTO.

Published here:

Updated here:

At a glance

Products

Meat and edible meat offal; Cereals

HS codes
  • 02 · Meat and edible meat offal
    • 02
  • 10 · Cereals
    • 10
Notifying member
European Union
Status
Corrected since it was notified
Objectives
  • Food safety
Area
SPS: Food safety, animal and plant healthSanitary and phytosanitary measures
Notification type
Regular notification
Document symbol
G/SPS/N/EU/959Latest notice: G/SPS/N/EU/959/Corr.1
Keywords
Food safety, Human health, Maximum residue limits (MRLs)

Key dates

Distributed by the WTO
Comment deadline
Closed on 25 August 2026
Proposed adoption
Proposed entry into force
This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union, and apply six months thereafter.

How to comment

The comment period closed on 25 August 2026. You can still raise concerns about the measure with your country's WTO SPS enquiry point, quoting the document symbol G/SPS/N/EU/959/Corr.1; it can take them up with the European Union.

Find your country's enquiry point on WTO ePing (opens in a new tab)

What the notification says

The proposed draft Regulation intends to lower all maximum residue levels (MRLs) for eight active substances which are no longer approved in the European Union: azocyclotin, chlorfenapyr, cyhexatin, dicofol, endosulfan, fenarimol, fenpropathrin and profenofos. Some MRLs are currently higher than the Limit of Quantification (LOQ). Codex maximum residue limits (CXLs) and import tolerance exist for some of them. For all active substances, EFSA has concluded that the TRVs cannot be confirmed since the data available were insufficient to meet the most recent data requirements. A stakeholder consultation was launched by EFSA allowing stakeholders to submit supporting information to confirm the TRVs. No relevant information was submitted. Therefore, as no TRVs could be set and consumer risk assessments could not be carried out, this draft Regulation proposes to lower to the LOQ all the MRLs for the eight non-approved active substances.

Notices on this measure

Every notice about this measure published here, newest first. Each one is the notifying member's own text.

  1. CorrigendumG/SPS/N/EU/959/Corr.1

    Maximum residue levels for azocyclotin, chlorfenapyr, cyhexatin, dicofol, endosulfan, fenarimol, fenpropathrin and profenofos in or on certain products

    This corrigendum corrects an error in Annex V of draft Commission Regulation amending Annexes II, III and V to Regulation (EC) No 396/2005 of the European Parliament and of the Council as regards maximum residue levels for azocyclotin, chlorfenapyr, cyhexatin, dicofol, endosulfan, fenarimol, fenpropathrin and profenofos in or on certain products (Text with EEA relevance), notified on 26 June 2026. In the Annex V, the MRL for fenpropathrin for the categories 0620000 to 0870990 is an unchanged (0.02*), whereas these categories should be marked 0.05*. The correct version of Annex V is the following:

    Open on WTO ePing (opens in a new tab)Official WTO document (opens in a new tab)Notified document (English) (opens in a new tab)

  2. Regular notificationG/SPS/N/EU/959

    Comment deadline: Closed on 25 August 2026

    Draft Commission Regulation amending Annexes II, III and V to Regulation (EC) No 396/2005 of the European Parliament and of the Council as regards maximum residue levels for azocyclotin, chlorfenapyr, cyhexatin, dicofol, endosulfan, fenarimol, fenpropathrin and profenofos in or on certain products (Text with EEA relevance)

    The proposed draft Regulation intends to lower all maximum residue levels (MRLs) for eight active substances which are no longer approved in the European Union: azocyclotin, chlorfenapyr, cyhexatin, dicofol, endosulfan, fenarimol, fenpropathrin and profenofos. Some MRLs are currently higher than the Limit of Quantification (LOQ). Codex maximum residue limits (CXLs) and import tolerance exist for some of them. For all active substances, EFSA has concluded that the TRVs cannot be confirmed since the data available were insufficient to meet the most recent data requirements. A stakeholder consultation was launched by EFSA allowing stakeholders to submit supporting information to confirm the TRVs. No relevant information was submitted. Therefore, as no TRVs could be set and consumer risk assessments could not be carried out, this draft Regulation proposes to lower to the LOQ all the MRLs for the eight non-approved active substances.

    Open on WTO ePing (opens in a new tab)Official WTO document (opens in a new tab)Notified document (English) (opens in a new tab)Notified document (English) (opens in a new tab)Notified document (English) (opens in a new tab)Notified document (English) (opens in a new tab)Notified document (English) (opens in a new tab)Notified document (English) (opens in a new tab)

Sources

Expodite writes its summary from the official record. The notification and the documents it notifies are on the WTO's own websites.

All updates from the European Union

  1. WTO notificationTBTProposed measure, open for comments

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    Symbol: G/TBT/N/EU/1251Comments until 2 January 2027

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    Symbol: G/SPS/N/EU/940/Add.1Comment period closed

  3. WTO notificationTBTProposed measure, open for comments

    Draft Commission Delegated Regulation amending Regulation (EC) No 1272/2008 of the European Parliament and of the Council as regards the harmonised classification and labelling…

    The purpose of this draft proposal for a Commission Delegated Regulation under Article 37(7) of Regulation (EC) No 1272/2008 on classification, labelling and packaging of substances and mixtures (the CLP Regulation) is to amend Table 3 of Part 3 of Annex VI to the CLP Regulation by introducing…

    No products listed by the notifying member

    Symbol: G/TBT/N/EU/1250Comments until 1 January 2027

  4. WTO notificationSPSProposed measure, open for comments

    Commission Implementing Regulation amending Implementing Regulation (EU) 2019/2072 as regards measures to prevent the entry into the Union territory, and the spread within it, of…

    Implementing Regulation 2019/2072 contains the list of Union quarantine pests, protected zone quarantine pests, and regulated non-quarantine pests (RNQPs). Furthermore, it lays down phytosanitary requirements for import and internal movement of plants, plant products and other objects that may…

    Symbol: G/SPS/N/EU/987Comments until 29 December 2026

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