Bellisai Giulia, Bernasconi Giovanni, Brancato Alba, Carrasco Cabrera Luis, 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 May 27;20(5):e07347. doi: 10.2903/j.efsa.2022.7347. eCollection 2022 May.
In accordance with Article 6 of Regulation (EC) No 396/2005, the applicant DuPont submitted a request to the competent national authority in Ireland to set an import tolerance for the active substance oxathiapiprolin in blueberries in support of an authorised use in the United States. The data submitted in support of the request were found to be sufficient to derive a maximum residue level (MRL) proposal for highbush blueberries by noting that lowbush blueberries () are excluded from the authorised use in the United States. Adequate analytical methods for enforcement are available to control the residues of oxathiapiprolin in plant matrices at the validated limit of quantification (LOQ) of 0.01 mg/kg. Based on the risk assessment results, EFSA concluded that the long-term intake of residues resulting from the use of oxathiapiprolin according to the reported agricultural practice 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，申请人杜邦向爱尔兰国家主管当局提交申请，请求设定蓝莓中活性物质恶唑菌酰胺的进口 tolerance，以支持其在美国的授权使用。支持该申请提交的数据被认为足以得出高丛蓝莓的最大残留限量（MRL）提案，同时注意到矮丛蓝莓被排除在美国的授权使用范围之外。有足够的执法分析方法来控制植物基质中恶唑菌酰胺的残留量，其验证定量限（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，按照报告的农业操作使用恶唑菌酰胺产生的残留物长期摄入不太可能对消费者健康构成风险。
