State
73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Daimler Trucks North America is recalling 2018-2019 Thomas Built school buses because brake caliper mounting bolts may be insufficiently tightened, increasing crash risk.
Great Dane is recalling 2019 Everest CL Multi-Temp trailers because loose brake adjuster anchor pins may cause brake failure or fire.
Daimler Trucks North America is recalling 2016-2019 Thomas Built Buses Minotour school buses because the rear emergency exit door may not open wide enough to meet federal safety standards.
Truck-Lite is recalling right-hand headlights for 2016-2019 International LT trucks due to incorrect markings that may lead to improper aiming and reduced visibility.
Collins is recalling 2011-2018 school buses because seat foam may not absorb enough impact in a crash, increasing injury risk.
JBS Tolleson is recalling approximately 6.9 million pounds of raw beef products potentially contaminated with Salmonella Newport. The recall follows an investigation linking the bacteria to 57 reported illnesses.
Toyota is recalling specific 2018-2019 Avalon, Sequoia, Tundra, and Avalon Hybrid vehicles because the air bag software may prevent deployment in a crash.
Suzuki is recalling 2017-2018 DL650, GSX-R1000, and GSX-S750 motorcycles because a twisted fuel pump O-ring may cause a fuel leak, increasing fire risk.
Toyota is recalling 2010-2014 Prius and 2012-2014 Prius V vehicles because excessive voltage may cause the hybrid system to shut down, increasing crash risk.
Altec is recalling 2017 AT37, AT41, and AT48 aerial devices because an incorrectly installed hose sock may cause electrical shock.
Yamaha is recalling 2012-2013 XTZ12 Super Tenere motorcycles because a gap in protective sealant may cause wire corrosion, preventing the engine from returning to idle and increasing crash risk.
BCI Burke is recalling about 200 Merge playground climbers because welded handgrips may create a strangulation hazard for children.
Hetero Labs Limited is recalling 98,016 bottles of Montelukast Sodium 10 mg tablets because one lot may contain Losartan Potassium 50 mg tablets.
Boston Scientific is recalling ESSENTIO pacemakers and CRT-P systems due to an elevated potential for early replacement caused by hydrogen-induced accelerated battery depletion.
Swanson Health Products is recalling Himalayan Crystal Salt because it may contain metal wire pieces. The product was distributed nationwide and in Canada and Switzerland.
Motor Coach Industries is recalling 2018-2019 MCI J4500 motorcoaches with 60-passenger seating due to insufficient emergency egress windows, which may delay passenger exit during an emergency.
Noven Pharmaceuticals is recalling Minivelle (estradiol) transdermal patches because the adhesive delivery system failed to meet specification standards for shear.
Boston Scientific is recalling specific ACCOLADE pacemakers and CRT-P systems due to an elevated potential for early replacement caused by hydrogen-induced accelerated battery depletion.
Boston Scientific is recalling PROPONENT pacemakers because hydrogen exposure may cause the battery to deplete faster than expected, requiring early replacement.
Biomet UK Ltd. is recalling specific HipLOC hip fracture fixation system plates due to an undersized bore that prevents the lag screw from fitting.
Agfa N.V. is recalling 108 DX-D 600 X-ray systems because support cables may break, posing a risk of the equipment falling.
GE Medical Systems is recalling 516 Discovery MR750w MRI systems because a small area on the bore surface can become warm enough to cause a serious burn if a patient touches it without proper padding.
Philips is recalling NTEGRIS Allura 9 0 FDXD systems because the ceiling monitor suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Philips is recalling AlIura Xper F010 F systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
CooperSurgical is recalling 18,000 units of Retractor System Elastic Stays because the sterile pouch seal may be compromised, increasing the risk of infection.