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.
Daimler Trucks North America is recalling 2017 Freightliner Cascadia and Western Star 5700 trucks because brittle axle output shafts may fracture, increasing crash risk.
Daimler Trucks North America is recalling 2016-2018 Thomas Built Buses Minotour school buses because occupant seats may lack reinforcement brackets, increasing injury risk in crashes.
Carrier and Bryant are recalling about 23,300 heat pumps because capacitors can fail, causing the units to overheat and pose a fire hazard.
Daimler Trucks North America is recalling 2013-2018 Thomas Built Saf-T-Liner HDX buses because seat lap belts may be anchored to the seat rather than the bus structure, increasing injury risk in a crash.
Nature's Truth is recalling Slow Release Iron 45 mg supplements because the bottles do not meet child-resistant closure requirements. Consumers should keep the product away from children and return it for a refund or replacement.
Volkswagen is recalling 2012-2014 Passat diesel vehicles because a short heat shield may allow grease to leak and contact hot exhaust parts, increasing fire risk.
Daimler Trucks North America is recalling 2013-2018 Thomas Built Saf-T-Liner HDX school buses because seat lap belts may be anchored to the seat rather than the bus structure.
Meridian Medical Technologies is recalling EpiPen auto-injectors because the delivery system may fail to activate, preventing patients from receiving epinephrine.
Killer Brownie Distributing LLC is recalling German Chocolate Killer Brownies due to undeclared peanuts, a potential allergen hazard.
Killer Brownie Distributing LLC is recalling Killer Brownie products due to undeclared peanuts. The mislabeled items were distributed to five states.
Killer Brownie Distributing LLC is recalling Original KB Killer Brownies due to undeclared peanuts. The product was distributed to Minnesota, New York, Ohio, Pennsylvania, and Wisconsin.
Meridian Medical Technologies is recalling EpiPen Jr. auto-injectors because the delivery system may fail to activate, preventing patients from receiving epinephrine.
Olympus is recalling 863 Endoeye HD II video telescopes because a damaged temperature sensor can cause the tip to become abnormally hot.
Killer Brownie Distributing LLC is recalling Peanut Butter KB Killer Brownies due to undeclared peanuts. The product was distributed to five states.
Temsa is recalling 2014-2017 TS45 motorcoaches because improper fasteners on the leveling valve linkage may loosen and detach, potentially damaging tires and increasing crash risk.
Medtronic is voluntarily recalling Newport HT70 and HT70 Plus ventilators because they may shut down spontaneously without an alarm during normal operation.
Sysmex America Inc is recalling XN-10 and XN-11 hematology analyzers due to a risk of fire caused by misaligned internal protective sheets.
Roche Diabetes Care is recalling specific versions of the Accu-Chek Connect app because a bug in the Bolus Advisor feature may provide incorrect insulin dosing advice.
Natus Medical is recalling neoBLUE 2 phototherapy lights sold from 2003 to 2008 to prevent the use of replacement boards that allow higher light intensity than originally cleared.
Sprague Devices is recalling Heavy-Duty Bus Pantograph Wiper Arms because the mounting casting may crack, causing the arms to bend or detach and reducing driver visibility.
Dale Medical Products is recalling Stabilock Endotracheal Adhesive Bases because the adhesive faceplate may lose its properties and fail to adhere to the patient's face.
Breg Inc is recalling 2,609 units of Dressing Rect L (P/N 02428) because some may have unsealed pouches, rendering them non-sterile.
Graco is recalling specific My Ride 65 convertible child seats because the webbing may not adequately restrain a child in a crash, increasing injury risk.
Weaver Popcorn Co. is recalling Trail's End Chicago sports collection snack tins due to potential Salmonella contamination.
Bard Peripheral Vascular Inc. is recalling 570 units of MR GHIATAS Beaded Breast Localization Wire because they may be non-MR compatible instead of MR compatible.