State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Chrysler is recalling 2011-2013 Dodge Durango and Jeep Grand Cherokee vehicles because sun visor wiring may short circuit, increasing the risk of a vehicle fire.
Ferrari is recalling 119 model year 2016 488 GTB vehicles because a fuel line connection may leak vapor, increasing fire risk.
BMW is recalling 2015 i8 vehicles because improperly drilled holes in the stability control unit may impair braking and handling, increasing crash risk.
Tiffin is recalling 2007-2015 motorhomes because a bolt on the electric steps may fracture, causing the steps to become unstable and increasing the risk of injury.
A. L. Schutzman Company, Inc. is recalling Ashdon Farms Honey Mustard Mix because the packaging lists whey but fails to declare milk in the 'Contains' statement.
Zenobia Co. is recalling My Spice Sage Ground Flax Seed Meal due to the possible presence of Salmonella. The product was sold nationwide via the internet.
Hyundai is recalling 2011-2012 Elantra vehicles because an electronic stability control sensor malfunction may cause unexpected braking and reduced engine power, increasing crash risk.
Remel Inc is recalling specific lots of Gentamicin Antimicrobial Susceptibility Testing Discs because the antibiotic concentration may be insufficient, potentially leading to incorrect test results.
Chrysler is recalling 2015 Jeep Compass and Patriot vehicles because a power steering hose clamp may be installed incorrectly, increasing the risk of a fire.
Insulet Corporation is recalling 5,179 boxes of OmniPod Insulin Management Systems because the needle mechanism may fail to deploy or deploy with a delay.
Kerry Foods is voluntarily recalling Sprinkle King Pink Sanding Sugar because it may contain metal. The product was distributed to 19 states.
A. L. Schutzman Company, Inc. is recalling Girl Scouts Honey Mustard Pretzel Mix because the product lists whey but fails to declare milk in the 'Contains' statement.
Insulet Corporation is recalling OmniPod Insulin Management Systems because the needle mechanism may fail to deploy or deploy with a delay.
Kerry Foods is voluntarily recalling Cinnamon Topical G4205 because it may contain metal. The recall covers 176,596 lbs distributed across 19 states.
GE Medical Systems is recalling 45 Optima IGS 320 systems due to a potential safety issue involving non-recoverable loss of displayed imaging.
Kerry Foods is voluntarily recalling Sprinkle King Black Sanding Sugar because it may contain metal. The product was distributed to 19 states.
Navistar is recalling certain 2007-2015 IC Bus transit models because wheelchair lift bearings may move out of position, causing the platform to fall.
Kerry Foods is voluntarily recalling specific lots of Sprinkle King Red Sanding Sugar and Red Sugar because they may contain metal.
MOOG Medical Devices Group is recalling EnteraLite Infinity Enteral Pump Delivery Sets because the purple ENFit connector may crack or break, causing leaks.
Kerry Foods is voluntarily recalling Sprinkle King Green Sanding Sugar in various sizes due to potential metal contamination. The recall covers 176,596 lbs distributed across 18 U.S. states.
Kerry Foods is voluntarily recalling Sprinkle King Lime Green Sanding Sugar because it may contain metal. The product was distributed to 18 states.
H&H Trailers is recalling 1,847 model year 2015-2016 trailers because aluminum gate hinges may bend or break, potentially causing the gate to open unexpectedly.
Stryker is recalling 120 units of Guidewire Introducer Needles shipped after expiration or with minimal time remaining due to infection risk.
Teleflex Medical is recalling 2,600 Hudson RCI Adult Universal Ventilator Circuits because the inspiratory and expiratory tubes are transposed.
Verathon is recalling GlideScope Video Laryngoscope blades because silicone adhesive may fail, causing the blade halves to separate during use.