Specific maximum levels of cross-contamination of antimicrobial active substances in non-target feed
Article 2
1. The specific maximum levels of cross-contamination in non-target feed for the antimicrobial active substances listed in Annex II to Regulation (EU) 2019/4 shall be set: (a) where the last batch manufactured, processed, stored or transported before the manufacturing, processing, storage or transport of the non-target feed is medicated feed, at 1 % of the antimicrobial active substance contained in that last batch of medicated feed, relative to a moisture content of 12 % in the non-target feed; (b) where the last batch manufactured, processed, stored or transported before the manufacturing, processing, storage or transport of the non-target feed is an intermediate product, at 1 % of the antimicrobial active substance to be contained in the medicated feed derived from that last batch of intermediate product, relative to a moisture content of 12 % in the non-target feed. 2. By way of derogation from paragraph 1, the specific maximum levels of cross-contamination in non-target feed for the antimicrobial active substances listed in Annex II to Regulation (EU) 2019/4 shall be set at the limit of quantification (‘LOQ’) laid down in the Annex to this Regulation, where the non-target feed is intended for the following animals: (a) food-producing animals other than fish where the non-target feed is manufactured, processed, stored or transported after the manufacturing, processing, storage or transport of medicated feed or intermediate products intended for aquaculture; (b) animals during the production of eggs or milk intended for human consumption; (c) food-producing animals intended for slaughter in the period for slaughter corresponding to the longest withdrawal period for the target animal species.