Modification of the existing maximum residue level for trifloxystrobin in honey

In accordance with Article 6 of Regulation (EC) No 396/2005, the applicant Bayer AG Crop Science Division submitted a request to the competent national authority in the Netherlands to set a maximum residue level (MRL) for the active substance trifloxystrobin in honey. The data submitted in support o...

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Published inEFSA journal Vol. 21; no. 8; pp. e08189 - n/a
Main Authors Bellisai, Giulia, Bernasconi, Giovanni, Carrasco Cabrera, Luis, Castellan, Irene, del Aguila, Monica, Ferreira, Lucien, Santonja, German Giner, Greco, Luna, Jarrah, Samira, Leuschner, Renata, Perez, Javier Martinez, Miron, Ileana, Nave, Stefanie, Pedersen, Ragnor, Reich, Hermine, Ruocco, Silvia, Santos, Miguel, Scarlato, Alessia Pia, Theobald, Anne, Tiramani, Manuela, Verani, Alessia
Format Journal Article
LanguageEnglish
Published United States John Wiley & Sons, Inc 01.08.2023
John Wiley and Sons Inc
Wiley
Subjects
Beekeeping
consumer risk assessment
Consumers
Crop science
Crops
Enforcement
Food safety
Fungicides
Health risks
Honey
Metabolites
MRL
Peer review
pesticide
Pesticides
Reasoned Opinion
Residues
Risk assessment
Toxicity
trifloxystrobin
Netherlands
consumer risk assessment
MRL
honey
pesticide
trifloxystrobin
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Summary:In accordance with Article 6 of Regulation (EC) No 396/2005, the applicant Bayer AG Crop Science Division submitted a request to the competent national authority in the Netherlands to set a maximum residue level (MRL) for the active substance trifloxystrobin in honey. The data submitted in support of the request were found to be sufficient to derive an MRL proposal for the commodity under assessment. An adequate analytical method for enforcement is available to control the residues of trifloxystrobin in honey 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 potential transfer of residues into honey assessed in the present MRL application of trifloxystrobin is unlikely to present a risk to consumer health. The consumer risk assessment shall be regarded as indicative and affected by uncertainties.
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Adopted: 12 July 2023
Question number EFSA‐Q‐2022‐00407
Acknowledgements EFSA wishes to thank: Stathis Anagnos, Andrea Mioč, Marta Szot, for the support provided to this scientific output.
Declaration of interest If you wish to access the declaration of interests of any expert contributing to an EFSA scientific assessment, please contact interestmanagement@efsa.europa.eu.
Requestor European Commission
EFSA may include images or other content for which it does not hold copyright. In such cases, EFSA indicates the copyright holder and users should seek permission to reproduce the content from the original source.
ISSN:1831-4732
1831-4732
DOI:10.2903/j.efsa.2023.8189