State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
McCormick & Co. is voluntarily recalling 18oz bottles of Stubb's Sticky Sweet BBQ Sauce due to glass defects that may cause chipped or missing glass.
Hormel Foods is recalling Great Shake Plus fortified nutrition drinks because they contain undeclared milk, a major food allergen.
Hormel Foods is recalling Great Shake and Great Shake Plus fortified nutrition drinks due to the presence of undeclared milk.
Siemens is recalling IMMULITE Progesterone test kits because DHEA-S causes falsely elevated results, potentially affecting diagnosis.
Robert Rothschild Farm LLC is recalling Gift Sets with Pretzel Twists because the product is not labeled with an ingredient statement, failing to declare soy and wheat allergens.
Ride The Ducks International LLC is recalling 1996-2014 amphibious vehicles because driver seats and seat belts may not secure occupants in a crash.
Hormel Foods is recalling Great Shake Plus fortified nutrition drinks because they contain undeclared milk. Consumers with this product should stop using it.
Parker Medical is recalling specific lots of Left Double Lumen Endobronchial Tubes because the single lung isolation feature did not function as intended.
Hormel Foods is recalling Great Shake and Great Shake Plus fortified nutrition drinks due to the presence of undeclared milk.
Hormel Foods is recalling Great Shake and Great Shake Plus fortified nutrition drinks because they contain undeclared milk.
The See Clear Company is recalling 119,829 units of color contact lenses because they may not be sterile and may have incorrect lot numbers or expiry dates.
Hormel Foods is recalling Great Shake and Great Shake Plus soy formula drinks because they contain undeclared milk.
Nu Skin Enterprises is voluntarily recalling Pharmanex Cortitrol capsules because they contain undeclared soy, a major food allergen.
Robert Rothschild Farm LLC is recalling Gift Sets with Chocolate Pretzel Dippers because the product is not labeled with an ingredient statement, failing to declare the allergens soy and wheat.
Siemens is recalling IMMULITE 2000 Progesterone kits because DHEA-S causes falsely elevated results, potentially affecting diagnosis.
Nu Skin Enterprises is voluntarily recalling Pharmanex Cholestin softgels because the product contains undeclared soy, a common allergen.
VanLeigh is recalling 2016-2017 Vilano fifth-wheel trailers because incorrect Federal Placard information may lead to vehicle overloading.
Villa Sistemi Medicali is recalling 65 Juno DRF x-ray systems because the footrest can detach from the table, causing patients to fall.
Advanced Sports International is recalling about 650 2017 Fuji bicycles because the rear wheel freehub can slip while pedaling, posing a fall hazard.
Trader Joe's is recalling Imported English Authentic Lemon Curd because it contains undeclared milk in the butter ingredient.
Nu Skin Enterprises is voluntarily recalling Pharmanex BioGinkgo tablets because they contain undeclared wheat, a major food allergen.
Mako Surgical Corporation is recalling 777 MAKO RIO THA Application User Guides because five AFMEA Risk Control Measures are missing from the documents.
Remel Inc is recalling Haemophilus Test Medium agar plates because poor organism growth may result in incorrect susceptibility test results.
Actavis Inc is recalling specific lots of Levofloxacin Ophthalmic Solution because the product failed impurity specifications for a related compound.
Teva Pharmaceuticals is recalling Risedronate Sodium Delayed-release Tablets because stability testing revealed low out-of-specification dissolution results.