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.
Mercedes-Benz is recalling specific 2016 C300 and C450 vehicles because the panoramic sunroof glass may not be properly bonded and could detach during operation.
Iowa Mold Tooling is recalling 2013-2016 Dominator vehicles because a valve bank cover may crack and fall off, creating a road hazard.
Transportation Collaborative is recalling 2012-2015 Trans Tech Student Safety Transporter school buses because the driver's side barrier may not deform properly in a crash.
Crescent Point Energy is recalling approximately 118 million gallons of propane gas in the U.S. because insufficient odorant levels may prevent consumers from detecting leaks, posing fire and burn risks.
Nuna Baby Essentials is recalling ZAAZ high chairs because the arm bar can bend or detach, posing a fall hazard to children.
Mercedes-Benz and Chrysler are recalling specific vehicles because the driver's frontal air bag inflator may rupture during deployment, potentially causing serious injury or death.
Volkswagen is recalling 2009 Routan vehicles because the air bag control unit may corrode and fail, potentially preventing air bag deployment or causing unintended deployment.
General Motors is recalling 2016 Chevrolet and GMC vehicles because the radio may fail to provide audio warnings for unbelted drivers or keys left in the ignition.
Starcraft RV is recalling 2016 Solstice and Travel Star trailers because water heaters may overheat, posing a scalding risk.
Mars Chocolate North America is recalling Dove Chocolate Assortment Snowflakes because the product may contain undeclared peanuts and egg ingredients.
Volkswagen Group of America is recalling specific 2007-2014 Volkswagen and Audi models because the driver's air bag inflator may rupture during deployment, potentially causing serious injury or death.
Draeger Medical is recalling Oxylog 2000 Plus ventilators because a software error can stop ventilation and trigger alarms.
Volkswagen is recalling 151,767 Audi and Volkswagen vehicles because the driver's airbag inflator may rupture during deployment, potentially causing serious injury.
Draeger Medical is recalling Oxylog 3000 and Oxylog 3000 Plus ventilators because a software error can stop ventilation and trigger alarms.
Daimler Vans is recalling 2007-2014 Dodge, Freightliner, and Mercedes-Benz Sprinter vans because the driver's air bag inflator may rupture during deployment.
Zatarain's is recalling Red Beans and Rice Original 8 oz. packages because they may contain an undeclared dairy allergen (milk).
Madison One Acme Inc. is recalling Tong Ren Tang Shenjing Shuairuo Wan because it contains unapproved human placenta, which may transmit disease.
Philips Medical Systems is recalling DS/US Proton Feature software due to a defect that may cause incorrect dose calculations in radiation therapy planning.
Philips is recalling Allura Xper FD20 OR Tables because live and still images may be misinterpreted, potentially affecting diagnostic accuracy.
Philips is recalling INTEGRIS and Allura medical imaging systems because a software issue may cause still images to be misinterpreted as live images.
Philips is recalling Allura Xper FD20 systems because still images may be misinterpreted as live images, potentially affecting diagnostic accuracy.
BioMerieux SA is recalling API ZYM Bx2 reagent because it produces false negative results, leading to discrepant identification outcomes in laboratory tests.
Pier 1 Imports is recalling Capella Island Swivel Dining Chairs because the base can break, posing a fall hazard to users.
Owens & Minor is recalling MediChoice sterile cohesive bandages because testing revealed microbial contamination.
Philips is recalling Allura Xper FD20 Biplane OR Tables because still images may be incorrectly interpreted as live images during use.