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.
Pharmaceutical Innovations, Inc. is recalling ElectroMist Electrode Conductivity Spray Solution due to potential failure in antimicrobial effectiveness testing.
Medline Industries is recalling 14,550 units of anti-fog solution in surgical kits because the chemical properties may have degraded, preventing proper defogging.
Pharmaceutical Innovations, Inc. is recalling ElectroMist electrode conductivity spray solution due to potential failure in antimicrobial effectiveness testing.
Lupin Pharmaceuticals is recalling 17,238 bottles of Gatifloxacin Ophthalmic Solution 0.5% because some bottles were found missing their labels.
Wilton Brands is voluntarily recalling 15,032 units of Chocolate Decorator Icing due to mold. The product was distributed in 35 states.
Teleflex Medical is recalling RUSCH CARE Premium Drain bags because the labels are not UDI compliant. The agency states this labeling issue is not likely to affect the device's function or performance.
Teleflex Medical is recalling RUSCH Urinary Drainage bags because the labels are not UDI compliant. The missing information does not affect the device's function or performance.
BMW is recalling 2019 X5 xDrive50i and X7 xDrive40i vehicles because left-side wheel bolts may loosen, increasing the risk of a crash.
Darsan Trading Co. is recalling HCI 100 matt black motorcycle helmets in size XL because they may not adequately protect the wearer in a crash.
The Boppy Company is recalling infant head and neck support accessories because the overstuffed design can tilt an infant's head forward, posing a suffocation risk.
MORryde is recalling certain Orbital and You Turn Rubber Pin Box Wedge Kits because incorrect bolt lengths may prevent proper tightening, increasing crash risk.
MORryde is recalling certain You Turn and Orbital Rotating Pin boxes because they may have shorter bolts than required, increasing the risk of a crash.
Hyundai is recalling 2018 Genesis G80 and 2017-2018 Genesis G90 vehicles because a loose seal may cause oil to leak onto the exhaust manifold, increasing fire risk.
Kia is recalling 2019 Optima vehicles because a software error may prevent the automatic emergency braking system from engaging when a stationary vehicle is detected.
Mercedes-Benz is recalling 2019-2020 vehicles because a software error in the radar sensor may impair Active Brake Assist, increasing crash risk.
Koch Foods is recalling approximately 743 pounds of breaded chicken bites because they contain undeclared soy, milk, and eggs.
Factory Direct Wholesale is recalling about 2,500 folding mattresses because they fail to meet the federal flammability standard, posing a fire hazard.
Golden State Medical Supply Inc. is recalling Losartan Potassium 100 mg tablets because an impurity called NMBA was detected in the active ingredient.
Macleods Pharma USA Inc. is recalling Losartan Potassium and Hydrochlorothiazide tablets because an impurity was detected in the active ingredient.
Becton Dickinson is recalling Alaris Pump Infusion Sets because a wall thickness variation can cause incomplete occlusion, potentially leading to unintended or faster-than-expected medication delivery.
GE Healthcare is recalling 28,094 Panda Infant Radiant Warmers because the bedside panels and latch areas can crack or break if the unit is moved using them instead of the designated handles.
Reyco is recalling Fire Truck Independent Front Suspensions because front shocks may separate and damage the steering gear, potentially causing a loss of power steering assist.
Teva Pharmaceuticals USA is recalling Losartan Potassium 50 mg tablets because an impurity was detected in the active ingredient.
Macleods Pharma USA Inc. is recalling Losartan Potassium and Hydrochlorothiazide tablets because an impurity was detected in the active pharmaceutical ingredient.
Major Pharmaceuticals is recalling Losartan Potassium 50 mg tablets because FDA testing found an impurity above acceptable levels.