Anastassiadou Maria, Brancato Alba, Carrasco Cabrera Luis, Greco Luna, Jarrah Samira, Kazocina Aija, Leuschner Renata, Magrans Jose Oriol, Miron Ileana, Nave Stefanie, Pedersen Ragnor, Raczyk Marianna, Reich Hermine, Ruocco Silvia, Sacchi Angela, Santos Miguel, Stanek Alois, Theobald Anne, Vagenende Benedicte, Verani Alessia
EFSA J. 2019 Jul 25;17(7):e05759. doi: 10.2903/j.efsa.2019.5759. eCollection 2019 Jul.
In accordance with Article 6 of Regulation (EC) No 396/2005, the applicant Du Pont de Nemours GmbH submitted two requests to the competent national authority in Ireland to modify the existing EU maximum residue levels (MRLs) and to set import tolerances for oxathiapiprolin in various plant commodities in order to accommodate the intended EU uses and the authorised uses of this active substance in China, Canada and the United States. The data submitted in support of the request were found to be sufficient to derive MRL proposals for all crops under consideration, except for Brussels sprouts and peas (without pods), for which residue data were either not submitted or were insufficient to support the use. Adequate analytical methods for enforcement are available to control the residues of oxathiapiprolin in commodities under consideration at the validated limit of quantification (LOQ) of 0.01 mg/kg. Based on the risk assessment results, EFSA concluded that, taking into account the existing and the intended uses, the long-term intake of residues of oxathiapiprolin is unlikely to present a risk to consumer health.
根据欧盟第396/2005号法规第6条，申请人杜邦德内穆尔有限公司向爱尔兰主管国家当局提交了两项请求，要求修改现有的欧盟最大残留限量（MRLs），并设定恶唑菌酰胺在各种植物商品中的进口容忍度，以适应欧盟的预期用途以及该活性物质在中国、加拿大和美国的批准用途。经审查，提交的支持该请求的数据足以得出所有正在审议作物的最大残留限量提案，但球芽甘蓝和豌豆（不带豆荚）除外，对于这两种作物，要么未提交残留数据，要么提交的数据不足以支持其使用。有足够的执法分析方法来控制正在审议商品中恶唑菌酰胺的残留量，验证定量限（LOQ）为0.01毫克/千克。基于风险评估结果，欧洲食品安全局得出结论，考虑到现有和预期用途，长期摄入恶唑菌酰胺残留不太可能对消费者健康构成风险。
