Anastassiadou Maria, Bellisai Giulia, Bernasconi Giovanni, Brancato Alba, Carrasco Cabrera Luis, Ferreira Lucien, Greco Luna, Jarrah Samira, Kazocina Aija, Leuschner Renata, Magrans Jose Oriol, Miron Ileana, Nave Stefanie, Pedersen Ragnor, Reich Hermine, Santos Miguel, Scarlato Alessia Pia, Theobald Anne, Vagenende Benedicte, Verani Alessia
EFSA J. 2021 May 6;19(5):e06578. doi: 10.2903/j.efsa.2021.6578. eCollection 2021 May.
In accordance with Article 6 of Regulation (EC) No 396/2005, the applicant Adama Agriculture B.V on behalf of Adama Makhteshim Ltd submitted a request to the competent national authority in France to modify the existing maximum residue levels (MRL) for the active substance folpet in barley, oat, rye and wheat. The data submitted in support of the request were found to be sufficient to derive MRL proposals for these commodities. Adequate analytical methods for enforcement are available to control the residues of folpet and phthalimide in dry commodities at the validated limit of quantification (LOQ) of 0.01 mg/kg per analyte. Based on the risk assessment results, EFSA concluded that the short-term and long-term intake of residues resulting from the use of folpet according to the reported agricultural practices is unlikely to present a risk to consumer health.
根据欧盟委员会第396/2005号法规第6条，申请人阿达玛农业有限公司（Adama Agriculture B.V）代表阿达玛马克西姆有限公司（Adama Makhteshim Ltd）向法国国家主管当局提交了一项请求，要求修改活性物质灭菌丹在大麦、燕麦、黑麦和小麦中的现有最大残留限量（MRL）。经审查，提交的支持该请求的数据足以得出这些商品的MRL提案。有足够的执法分析方法来控制干燥商品中灭菌丹和邻苯二甲酰亚胺的残留量，每种分析物的验证定量限（LOQ）为0.01 mg/kg。基于风险评估结果，欧洲食品安全局（EFSA）得出结论，按照报告的农业实践使用灭菌丹产生的残留物短期和长期摄入不太可能对消费者健康构成风险。
