State
73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Pfizer is recalling 17,136 bottles of Children's Advil Suspension because the included dosage cup is marked in teaspoons while the label instructions use milliliters.
Validus Pharmaceuticals is recalling 7,864 bottles of Calcitriol Oral Solution because testing showed lower than expected potency at the 18-month stability time point.
Akorn, Inc. is recalling specific lots of Azelastine HCl Ophthalmic Solution 0.05% because of out-of-specification results for Azelastine N-oxide.
Validus Pharmaceuticals is recalling 696 bottles of Rocaltrol (calcitriol) Oral Solution because testing showed lower than expected potency.
Mayne Pharma is recalling 6,456 bottles of Oxycodone and Acetaminophen Tablets due to a lot number labeling error on the primary container.
Collins Bus is recalling 2012-2018 school buses with Ricon wheelchair lifts because a cam may fail, causing the platform to rise too high and increasing injury risk.
Midwest Fire is recalling 2017-2019 emergency vehicles because Whelen brake lights may illuminate without the brake pedal being pressed, potentially confusing other drivers.
Bridgestone is recalling specific commercial tires because exposed sidewall steel cords can cause rapid air loss, increasing crash risk.
Ford is recalling 2015-2018 F-150 Regular Cab and SuperCrew Cab vehicles because seat belt pretensioner sparks may ignite B-pillar materials, posing a fire risk.
Daimler Trucks is recalling 2016-2019 FCCC chassis because a damaged module may cause rear lights to fail, increasing crash risk.
Eldorado is recalling 2012-2018 transit buses because a wheelchair lift cam may fail, allowing the platform to rise too high and increase injury risk.
General Motors is recalling 2015-2016 Chevrolet and GMC vehicles because a brake pedal pivot nut may loosen, potentially rendering the brakes inoperative or interfering with the accelerator.
Daimler Trucks is recalling 2017-2019 Freightliner and Western Star trucks because a restricted fuel pump cooling circuit screen may cause the fuel line to burst, leading to fuel leaks or engine stalling.
General Motors is recalling 2018-2019 Chevrolet, GMC, Buick, and Cadillac vehicles because rear brake caliper pistons may have insufficient coating, potentially reducing braking performance.
Kawasaki is recalling 2018 Ninja H2 SX SE motorcycles because a center stand spring pin may detach, causing the stand to drag and increasing crash risk.
Jayco is recalling 2018 Alante vehicles because damaged leveling system hydraulic hoses may leak fluid onto the exhaust system, increasing the risk of a fire.
PetSmart is recalling 20-inch and 30-inch reptile strip light fixtures because the bulbs can overheat and ignite the hood, posing a fire hazard.
Core Health & Fitness is recalling StairMaster 8G Gauntlet Stepmill machines because the steps can accelerate rapidly without user input, posing a fall hazard.
Micro Bird is recalling 2012-2018 school buses with specific wheelchair lifts because a cam may fail, allowing the platform to rise too high and increase injury risk.
Brown Industries is recalling 2017-2018 American Heritage Trolley buses because a wheelchair lift component may fail, causing the platform to rise too high and increasing injury risk.
Champion is recalling 2012-2018 buses with specific wheelchair lifts where a cam may fail, allowing the platform to rise too high and risk injury.
Westminster Pharmaceuticals is recalling specific lots of Levothyroxine and Liothyronine tablets because they failed content uniformity specifications due to an adulterated ingredient.
Westminster Pharmaceuticals is recalling Levothyroxine and Liothyronine tablets because they failed content uniformity specifications due to an adulterated ingredient and poor manufacturing controls.
Westminster Pharmaceuticals is recalling Levothyroxine and Liothyronine tablets because they failed content uniformity specifications due to an adulterated ingredient and poor manufacturing controls.
Gift Services Inc is recalling Sherman Candy Caramels found in specific gourmet gift baskets due to undeclared pecans, walnuts, almonds, and/or peanuts.