State
73,737 recalls have nationwide distribution and so reach Minnesota. 7,849 additional recalls listed Minnesota specifically in their distribution scope.
Of the 7,849 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 2,245 (29%) are Severe.
Which agencies issued them
These figures cover only the 7,849 recalls whose distribution notice names Minnesota specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Plant Therapy is recalling specific wintergreen essential oils and blends because the packaging is not child-resistant, posing a risk of poisoning to young children.
BMW is recalling specific 2018-2020 motorcycles because the brake fluid reservoir cap may not clearly state the required fluid type, potentially leading to improper maintenance.
CPSC recalls about 3,600 Kids & Koalas baby walkers sold on Amazon due to fall and neck entrapment risks.
BMW is recalling specific motorcycle brake fluid reservoir caps because they may not clearly state the required brake fluid type, potentially leading to improper maintenance.
Woom bikes USA is recalling approximately 5,500 model 4, 5, and 6 bicycles because the front fork can loosen and detach, posing fall and injury risks.
C3 Manufacturing is recalling about 1,100 Perfect Descent Auto Belay climbing devices because the belay can loosen, causing rope slack and allowing the climber to fall.
Kawasaki is recalling approximately 80,000 MULE PRO off-highway utility vehicles because excessive steering shaft wear can affect steering control, posing a crash hazard.
Bentley is recalling 2018-2020 Bentayga vehicles with third-row seats because the upper seat belt attachment may detach in a crash, increasing injury risk.
Qiagen is recalling Rotor-Gene Q instruments with software version 2.3.4 because a bug causes concentration results to be reported as logarithmic values, potentially leading to false negative test results.
American Health Packaging is recalling 53,619 cartons of Ranitidine Tablets, 150 mg, due to potential N-Nitrosodimethylamine (NDMA) amounts above FDA-established levels.
Precision Dose Inc. is recalling Ranitidine Oral Solution because the active ingredient contained the impurity N-nitrosodimethylamine (NDMA).
Maquet Cardiovascular is recalling Getinge 88-Series washer disinfectors because ruptured spot welds may cause water leakage, posing slip and infection risks.
Cardinal Health is recalling Monoject Hypodermic Safety Needles that were shipped as non-sterile but labeled as sterile. The firm is not aware of any patient harm.
Daimler Vans USA is recalling 2019 Mercedes-Benz and Freightliner Sprinter vans because winter tires may be installed incorrectly, reducing traction in wet or snowy conditions.
Daimler Vans is recalling 2018-2019 Mercedes-Benz and Freightliner Sprinter vehicles because the spare tire label may list the maximum speed in kilometers per hour instead of miles per hour.
H J Harkins Company Inc is recalling Acetaminophen 500 mg tablets because a foreign Women's Prenatal tablet was found in the product.
Cardinal Health is recalling Monoject 3mL syringes with safety needles because they were shipped as non-sterile despite labeling. The firm is not aware of any patient harm reports.
Earth Sonnets is recalling Wintergreen Essential Oil because the packaging is not child-resistant, posing a risk of poisoning to young children.
Stonewall Kitchen is recalling Ghost Pepper Salsa because it contains undeclared milk and soy allergens. Consumers should check their pantry for the specific product.
Lamborghini is recalling 26 2020 Aventador SVJ vehicles because the interior door handle mechanism may fail, preventing the door from opening from inside.
SeeNext Venture is recalling NumbSkin pain relief cream because the packaging is not child-resistant, posing a risk of poisoning to young children.
Daimler Vans USA is recalling 2018-2019 Sprinter vans because the spare tire may lack a maximum speed label, increasing the risk of tire failure.
Medicrea International is recalling 3,529 Iliac Screws because an internal component was assembled incorrectly, which may cause the tulip head to disengage from the shank.
Medtronic is recalling six Simulus 850 Semi Rigid Ring/Band Accessory Kits because demonstration units may have contacted porcine tissue.
Earthroma is recalling Wintergreen Essential Oil bottles because the packaging is not child-resistant, posing a poisoning risk to young children.