State
73,827 recalls have nationwide distribution and so reach Minnesota. 7,851 additional recalls listed Minnesota specifically in their distribution scope.
Of the 7,851 recalls naming Minnesota we have scored against our rubric, 1,137 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,246 (29%) are Severe.
Which agencies issued them
These figures cover only the 7,851 recalls whose distribution notice names Minnesota specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Iowa Select Herbs LLC is recalling Alfalfa Leaf products under a consent decree because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling alcohol-free Sage Leaf products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Kava Kava Root products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Lobelia Leaf products under a consent decree because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Nettle Leaf dietary supplements because they are misbranded, unapproved new drugs, and adulterated.
Iowa Select Herbs LLC is recalling Papaya Leaf products under a consent decree because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Bayberry Root products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling White Willow Bark products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Grape Seed Leaf products under a consent decree because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Elderberry Fruit products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Sassafras Root Bark because it is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling 4 fl. oz. bottles of Scullcap (Scutellaria lateriflora) because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Alisma Leaf products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Fennel Seed under a consent decree because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Cudweed products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Yucca Root under a consent decree because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Valerian Root under a consent decree because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Fenugreek Seed because it is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Iowa Select Herbs LLC is recalling Cinnamon Bark products under a consent decree because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling Burdock Root under a consent decree because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Fujifilm Medical Systems is recalling 2,062 Smart CR Digital Computed Radiography Systems due to reports of power supply failure.
Iowa Select Herbs LLC is recalling Ginger Root products under a consent decree because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Iowa Select Herbs LLC is recalling 10 bottles of 4 fl. oz. Aloe Vera Juice because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Mako Surgical Corporation is recalling 10 units of the MAKOplasty Hip Array Kit Laminate 150230 because the product may list two part numbers for the RIO Base Array.
Iowa Select Herbs LLC is recalling Schizandra Berry under a consent decree because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.