Bellisai Giulia, Bernasconi Giovanni, Brancato Alba, Cabrera Luis Carrasco, Castellan Irene, Ferreira Lucien, Giner German, Greco Luna, Jarrah Samira, Leuschner Renata, Magrans Jose Oriol, Miron Ileana, Nave Stefanie, Pedersen Ragnor, Reich Hermine, Robinson Tobin, Ruocco Silvia, Santos Miguel, Scarlato Alessia Pia, Theobald Anne, Verani Alessia
EFSA J. 2022 Aug 9;20(8):e07527. doi: 10.2903/j.efsa.2022.7527. eCollection 2022 Aug.
In compliance with Article 43 of Regulation (EC) No 396/2005, EFSA received a mandate from the European Commission to perform a targeted review of the maximum residue levels (MRLs) for indoxacarb based on Codex maximum residue limits (CXLs) or on import tolerances which might still be maintained after the expire of the approval of the active substance. EFSA screened the existing MRLs based on CXLs or on import tolerances considering the new toxicological reference values established during the peer review process for the renewal of the approval of indoxacarb and identified the MRLs for which an acute risk could not be excluded and several MRLs that are unlikely to pose a risk for consumers. Fall-back MRLs could not be proposed for the commodities exceeding the new toxicological reference values as no further data were provided during the call for data. Therefore, risk managers may consider maintaining only the MRLs identified during the screening as safe for consumers. However, for some of the proposed MRLs, further consideration by risk managers is needed due to the uncertainties identified.
根据欧盟委员会(EC)第396/2005号法规第43条,欧洲食品安全局(EFSA)接到欧盟委员会的任务,要基于食品法典委员会最大残留限量(CXLs)或基于活性物质批准到期后仍可能维持的进口容忍度,对茚虫威的最大残留限量(MRLs)进行针对性审查。欧洲食品安全局根据CXLs或进口容忍度筛选现有MRLs,同时考虑在茚虫威批准续期的同行评审过程中确立的新毒理学参考值,并确定了无法排除急性风险的MRLs以及几个不太可能对消费者构成风险的MRLs。对于超过新毒理学参考值的商品,由于在征集数据期间未提供更多数据,因此无法提出替代MRLs。因此,风险管理者可考虑仅保留在筛选过程中确定的对消费者安全的MRLs。然而,对于一些提议的MRLs,由于存在不确定性,风险管理者需要进一步考虑。