美国食品和药物管理局召回了6000多个M&Ms单位,因为未申报的花生,牛奶和大豆过敏原;没有报告的疾病. FDA recalls 6,000+ M&M’s units over undeclared peanut, milk, and soy allergens; no illnesses reported.

美国食品和药物管理局已召回20个州销售的6000多件重新包装的M&M's花生和经典糖果,原因是未申报的过敏原,包括牛奶,大豆和花生. The FDA has recalled over 6,000 units of repackaged M&M’s Peanut and classic candies sold in 20 states due to undeclared allergens, including milk, soy, and peanuts. 自愿召回,由Beacon Promotions Inc.于1月26日发起,并于2月4日更新,涵盖了以Make Your Mark,Subaru,Adobe和马里兰大学等名称标记的产品,商品号为BB458BG和BB471BG,批量代码,最好到2026年9月为止. The voluntary recall, initiated by Beacon Promotions Inc. on January 26 and updated February 4, covers products labeled under names like Make Your Mark, Subaru, Adobe, and University of Maryland, with item numbers BB458BG and BB471BG, lot codes, and best-by dates through September 2026. 美国食品和药物管理局将召回产品归类为II类,表明可能会产生暂时或可逆的健康影响,尽管没有报告任何疾病. The FDA classified the recall as Class II, indicating a potential for temporary or reversible health effects, though no illnesses have been reported. 促请消费者检查标签,在对所列成分过敏时避免被召回的物品,并返回或丢弃这些物品。 Consumers are urged to check labels, avoid the recalled items if allergic to the listed ingredients, and return or discard them. 问题起源于第三方重新包装过程中的不当标签,而不是原产品。 The issue stems from improper labeling during third-party repackaging, not the original product.