State
73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ardent Mills is voluntarily recalling specific lots of Hilltop Hearth Self-Rising Flour because they may be contaminated with Salmonella.
Boston Scientific is recalling 49 Stingray Guidewires that are 185cm but incorrectly labeled as 300cm. The mislabeling could lead to improper use during angioplasty procedures.
Lupin Pharmaceuticals is recalling Lovastatin 40 mg tablets because the drug substance used was out of specification for impurity results.
Ortho Clinical Diagnostics is recalling Vitros Myoglobin Calibrators due to a stability issue that may cause calibration failures or atypical quality control results.
Advanced Pharma Inc. is recalling Oxytocin 30 Units Injectable Solution because the product may contain higher concentrations than labeled.
Akorn Inc is recalling specific lots of Moisturizing Lubricant Eye Drops because they failed stability specifications for Sodium Perborate.
Smiths Medical ASD Inc. is recalling arterial blood sampling kits because the included povidone iodine prep pads may not maintain potency through their expiration dates.
Akorn Inc. is recalling specific lots of Clobetasol Propionate Emollient Cream 0.05% because stability testing revealed out-of-specification preservative levels.
Advanced Pharma Inc. is recalling 672 bags of Oxytocin 20 Units Injectable Solution because the product may contain higher concentrations than labeled.
Smiths Medical ASD Inc. is recalling Portex Pulsator Arterial Blood Sampling Kits because the included povidone iodine prep pads may not maintain potency through their expiration dates.
Perrigo New York, Inc. is recalling specific lots of Ciclopirox shampoo 1% because stability testing revealed out-of-specification related substances.
Advanced Pharma Inc. is recalling 12 bags of Oxytocin 10 Units Injectable Solution because the product may contain higher concentrations than labeled.
ACP Nimble Buyer, Inc. is recalling Mometasone Furoate Cream due to a typographical error in the National Drug Code (NDC) on the label.
Navistar is recalling 2016-2020 International LT and 2017-2018 Prostar trucks because a cracked exhaust bracket could cause the tailpipe to detach, creating a road hazard.
Mercedes-Benz is recalling 2018-2019 GLA 250 vehicles because an incorrect rear seat covering may hide the center child seat anchor point, increasing crash injury risk.
Mercedes-Benz is recalling 2018 CLA 250 and CLA 250 4MATIC vehicles because tail and side marker lights may flicker or fail, increasing crash risk.
Mercedes-Benz is recalling 2017-2018 C and E Class vehicles because front seatbacks may not lock properly, increasing injury risk in a crash.
JumpSport is recalling about 11,300 half-fold fitness mini-trampolines because the folding frame can forcefully hit users, causing cuts, bruises, and dental injuries.
Keystone RV is recalling certain 2018-2019 recreational trailers because cargo tray rivets may shear, allowing the tray to detach and potentially injure someone.
New England Wheels is recalling 2008, 2013, and 2014 Ford E-250 vans with Ricon wheelchair lifts because the positioning cam may fail, causing the platform to rise too high.
D&D Futon Furniture is recalling about 800 Sleeper Chair Folding Foam Beds because they fail to meet federal flammability standards, posing a fire hazard.
Foundation Ambulance is recalling 2017-2018 Type I and III ambulances because brake lights may illuminate without the pedal being pressed, potentially confusing other drivers.
Takata is recalling certain driver frontal air bag inflators that may rupture due to propellant degradation, posing a risk of serious injury or death.
Jayco is recalling 2019 Embark motorhomes because missing or improperly installed cotter pins may cause brake actuator rods to detach, increasing stopping distance and crash risk.
Meritor is recalling specific EX225 disc brake calipers because cracked drive pins may fracture, causing the vehicle to pull to one side while braking and increasing crash risk.