2025年3月25日，歐盟食品安全局（EFSA）發布消息稱，擬修訂溴氰菊酯（deltamethrin）在櫻桃中的最大殘留限量。
根據歐盟條例（EC）No 396/2005第6章的規定，Bayer SAS提交了該修訂申請。經過評估，歐盟食品安全局得出結論，短期和長期攝入因使用溴氰菊酯而產生的殘留物不太可能對消費者健康構成風險。部分原文報道如下：
In accordance with Article 6 of Regulation (EC) No 396/2005, the applicant Bayer SAS submitted a request to the competent national authority in France to modify the existing maximum residue level (MRL) for the active substance deltamethrin in cherries. The data submitted in support of the request were found to be sufficient to derive a MRL proposal for cherries. Adequate analytical methods for enforcement are available to control the residues of deltamethrin on the commodity under consideration at the validated limit of quantification (LOQ) of 0.01 mg/kg. based on the risk assessment results, EFSA concluded that the short-term and long-term intake of residues resulting from the use of deltamethrin according to the reported agricultural practices is unlikely to present a risk to consumer health. The risk assessment shall be regarded as indicative and affected by non-standard uncertainties, due to the lack of information on the actual occurrence of residues of trans-deltamethrin and alpha-R-deltamethrin in certain crops and on the toxicological profile of both isomers. Furthermore, also information on the metabolism of these isomers in livestock and adequate livestock feeding studies in cows and hens, investigating residues in all relevant tissues and matrices according to the residue definitions for monitoring and risk assessment simultaneously, are still missing.
根據歐盟條例（EC）No 396/2005第6章的規定，Bayer SAS提交了該修訂申請。經過評估，歐盟食品安全局得出結論，短期和長期攝入因使用溴氰菊酯而產生的殘留物不太可能對消費者健康構成風險。部分原文報道如下：
In accordance with Article 6 of Regulation (EC) No 396/2005, the applicant Bayer SAS submitted a request to the competent national authority in France to modify the existing maximum residue level (MRL) for the active substance deltamethrin in cherries. The data submitted in support of the request were found to be sufficient to derive a MRL proposal for cherries. Adequate analytical methods for enforcement are available to control the residues of deltamethrin on the commodity under consideration at the validated limit of quantification (LOQ) of 0.01 mg/kg. based on the risk assessment results, EFSA concluded that the short-term and long-term intake of residues resulting from the use of deltamethrin according to the reported agricultural practices is unlikely to present a risk to consumer health. The risk assessment shall be regarded as indicative and affected by non-standard uncertainties, due to the lack of information on the actual occurrence of residues of trans-deltamethrin and alpha-R-deltamethrin in certain crops and on the toxicological profile of both isomers. Furthermore, also information on the metabolism of these isomers in livestock and adequate livestock feeding studies in cows and hens, investigating residues in all relevant tissues and matrices according to the residue definitions for monitoring and risk assessment simultaneously, are still missing.
