Kommisjonsforordning (EU) 2024/246 av 16. januar 2024 om endring av vedlegg IV til til europaparlaments- og rådsforordning (EF) nr. 396/2005 med hensyn til Pythium oligandrum stamme M1, Trichoderma atroviride stamme AGR2 og Trichoderma atroviride stamme AT10
Øvre grenseverdier for rester av plantevernmidler i næringsmidler: endringsbestemmelser
Kommisjonsforordning publisert i EU-tidende 17.1.2024
Tidligere
- Utkast til kommisjonsforordning sendt til Europaparlamentet og Rådet for klarering og publisert i EUs komitologiregister 17.10.2023
Nærmere omtale
BAKGRUNN (fra kommisjonsforordningen)
(1) For Pythium oligandrum strain M1, Trichoderma atroviride strain AGR2 and Trichoderma atroviride strain AT10, no specific maximum residue levels (‘MRLs’) have been set. Therefore, for those active substances the default value of 0,01 mg/kg laid down in Article 18(1), point (b), of Regulation (EC) No 396/2005 applies.
(2) Commission Implementing Regulation (EU) 2022/23142 renewed the approval of the active substance Pythium oligandrum strain M1. During the peer review of the pesticide risk assessment of the active substance under Regulation (EC) No 1107/2009, the European Food Safety Authority (‘the Authority’) concluded that some information was not available as regards the dietary risk assessment for consumers and that further consideration by risk managers was required. As set out in the renewal report for that active substance in the context of the risk assessment under Regulation (EC) No 1107/2009, Pythium oligandrum strain M1 is not pathogenic to humans, is not expected to produce toxins that are relevant for human health and the risk to humans through metabolites is negligible. Taking into account the peer review of the pesticide risk assessment of the active substance Pythium oligandrum strain M1, the renewal report and Article 5 and Article 14(2), points (a), (c) and (d), of Regulation (EC) No 396/2005, there is no need to establish MRLs for this active substance and it is therefore appropriate to include Pythium oligandrum strain M1 in Annex IV to Regulation (EC) No 396/2005.
(3) Commission Implementing Regulation (EU) 2023/2166 approved the low-risk active substance Trichoderma atroviride strain AGR2. During the peer review of the pesticide risk assessment of the active substance under Regulation (EC) No 1107/2009, the Authority concluded7 that some information was not available as regards the dietary risk assessment for consumers and that further consideration by risk managers was required. As set out in the review report for that active substance8 in the context of the risk assessment under Regulation (EC) No 1107/2009, Trichoderma atroviride strain AGR2 is not pathogenic to humans, is not expected to produce toxins that are relevant for human health and the risk to humans through metabolites is negligible. Taking into account the peer review of the pesticide risk assessment of the active substance Trichoderma atroviride strain AGR2, the review report and Article 5 and Article 14(2), points (a), (c) and (d), of Regulation (EC) No 396/2005, there is no need to establish MRLs for this active substance and it is therefore appropriate to include Trichoderma atroviride strain AGR2 in Annex IV to Regulation (EC) No 396/2005.
(4) Commission Implementing Regulation (EU) 2023/1999 approved the low-risk active substance Trichoderma atroviride strain AT10. During the peer review of the pesticide risk assessment of the active substance under Regulation (EC) No 1107/2009, the Authority concluded10 that some information was not available as regards the dietary risk assessment for consumers and that further consideration by risk managers was required. As set out in the review report for that active substance11 in the context of the risk assessment under Regulation (EC) No 1107/2009, Trichoderma atroviride strain AT10 is not pathogenic to humans, is not expected to produce toxins that are relevant for human health and the risk to humans through metabolites is negligible. Taking into account the peer review of the pesticide risk assessment of the active substance Trichoderma atroviride strain AT10, the review report and Article 5 and Article 14(2), points (a), (c) and (d), of Regulation (EC) No 396/2005, there is no need to establish MRLs for this active substance and it is therefore appropriate to include Trichoderma atroviride strain AT10 in Annex IV to Regulation (EC) No 396/2005.
(5) Regulation (EC) No 396/2005 should therefore be amended accordingly. (6) The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on Plants, Animals, Food and Feed,