State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Mack is recalling certain 2012-2017 trucks because front wheel hubs may fail, potentially causing loss of vehicle control or dropped parts.
Kovatch Mobile Equipment Corp. is recalling certain KME fire trucks because water may leak into the ladder position sensor, increasing the risk of injury.
ARBOC is recalling 2015-2016 Spirit of Liberty transit buses because the parking brake may engage unexpectedly while driving, increasing crash risk.
Pierce Manufacturing is recalling 2015-2016 Dash CF emergency vehicles because a defective bracket may damage the starter motor, increasing the risk of a fire.
Ford is recalling specific 2016-2017 Taurus, Flex, MKT, and Explorer vehicles because improperly brazed turbocharger tubes may leak oil, increasing fire risk.
KME is recalling certain Predator SS Aerial and Predator Aerial vehicles because rear brakes may engage without the pedal being pressed, increasing crash and fire risk.
Volvo is recalling certain 2013-2017 VNL, VNM, and 2017 VNX trucks because incorrect software may allow oil and water to contaminate the brake system, potentially affecting braking performance.
Volvo is recalling 2017 VHD, VNL, and VNM trucks because front wheel hubs may fail, risking loss of vehicle control.
Chrysler is recalling specific 2009 Dodge Durango, Chrysler Aspen, and 2010 RAM 3500 vehicles because the driver's air bag inflator may rupture during deployment, posing a risk of serious injury.
4 Sizzle LLC is recalling approximately 1,700 wooden barrel-shaped charcoal grills with the Shock Top logo due to a fire hazard. The grills were distributed as promotional items and display enhancers.
C&M is recalling 2016 5x10 Cargo Trailers because they may lack required license plate illumination, increasing crash risk.
Two Chefs On A Roll is recalling Trader Joe's White Bean & Basil Hummus due to potential Listeria monocytogenes contamination.
Troyer Cheese Inc is recalling Backroad Country Walnuts Halves & Pieces due to potential Listeria monocytogenes contamination. The product was distributed to 26 states.
Back to Nature Foods is recalling Dark Chocolate Coconut Granola because it contains undeclared milk.
Back To Nature Foods is recalling specific lots of Chocolate Chunk Cookies because they contain undeclared milk.
Troyer Cheese Inc is recalling Backroad Country Cranberry Nut Delight Mix due to potential Listeria monocytogenes contamination.
Two Chefs On A Roll, Inc. is recalling Trader Joe's Mediterranean Hummus due to potential Listeria monocytogenes contamination.
American Blue Ribbon Holdings is recalling 7,273 Ultimate Chocolate Chip Cookie Dough Pies because the cookie dough may be contaminated with Listeria monocytogenes.
Back to Nature Foods is recalling specific lots of Gluten-Free Chocolate Delight Granola because the product contains undeclared milk.
Cantrell Drug Company is recalling Fentanyl Citrate bags due to a lack of assurance of sterility. The recall affects 2,545 bags distributed nationwide.
Cantrell Drug Company is recalling 2,509 single-dose Hydromorphone HCl syringes nationwide due to a lack of assurance of sterility.
Cantrell Drug Company is recalling 5,067 syringes of Rocuronium Bromide 50 mg/5 mL injection solution nationwide due to a lack of assurance of sterility.
Cantrell Drug Company is recalling 471 bags of Fentanyl Citrate 1,500 mcg in 0.9% Sodium Chloride due to a lack of assurance of sterility.
Troyer Cheese Inc is recalling Backroad Country Honey Island Crunch Mix due to potential Listeria monocytogenes contamination. The product was distributed to 26 states.
Cantrell Drug Company is recalling specific lots of Glycopyrrolate injection because the firm cannot assure the sterility of the product.