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.
Chrysler is recalling 2018-2019 RAM 1500 trucks because the rear differential may be underfilled, which could cause axle failure and increase crash risk.
Daimler Trucks North America is recalling 2017-2019 Thomas Built Buses Saf-T-Liner C2 school buses because seat mounting feet may pull through the floor joint in a crash.
Autocar is recalling 297 Xspotter vehicles from 2018-2019 because an incorrectly welded brake pedal mounting plate could cause the pedal to disconnect, increasing crash risk.
BMW is recalling 2017-2019 MINI Countryman vehicles because a missing crash protection plate near the fuel pump could cause a fuel leak and fire risk in a crash.
American Landmaster is recalling about 1,500 off-road utility vehicles because gas can leak from the tank, posing fire and burn hazards.
Daimler Trucks is recalling 2015-2019 Thomas Built Buses equipped with specific wheelchair lifts because a component may fail, allowing the platform to rise too high.
Manhattan Toy is recalling Pull-Back Speedy Jets because rubber tires can separate, posing a choking hazard for young children.
Vornado Air is recalling VH101 Personal Vortex electric space heaters because they can overheat, posing fire and burn hazards. One death and 19 fire reports have been linked to the units.
Spacelabs Healthcare is recalling 328 Arkon Anesthesia Delivery Systems because they may stop providing mechanical ventilation while in use or idle.
Altec Industries is recalling 2008-2018 Aerial Devices with aluminum work platforms because mounting holes may fail, causing unexpected movement and injury risk.
Volvo is recalling 2019 XC40 vehicles because brake pedals may not be correctly riveted, potentially reducing braking performance and increasing crash risk.
NxStage Medical is recalling Express Fluid Warmers due to a potential risk of electrical fire if fluid leaks into the power receptacle.
Beekley Corporation is recalling TomoSPOT skin markers used in mammography because they may create imaging artifacts that mimic calcifications on patient mammograms.
Beekley Corporation is recalling O-SPOT REF 791 and 791S skin markers because they may create imaging artifacts that mimic calcifications on mammograms.
Hamilton Medical AG is recalling two Hamilton-C3 ventilators because an out-of-specification control board component may cause the device to shut down and trigger alarms.
Yamaha is recalling about 120 SRVenture DX snowmobiles because loose passenger handgrips could cause falls and severe injury.
Mevion Medical Systems is recalling seven MEVION S250 and S250i proton beam therapy systems due to unauthorized accessory combinations that may cause patient injury.
Hamilton Medical AG is recalling 16 Hamilton-C1 ventilators because a defective control board component may cause the device to shut down and trigger alarms.
Saratoga Food Specialties is voluntarily recalling Pizza Hut Seasoning Breadsticks because a supplier recalled dry whey powder due to potential Salmonella presence.
Altec is recalling 2017-2018 LS63 Aerial Devices because an incorrectly placed battery fuse may increase the risk of an electrical short and fire.
Withings is recalling Nokia BPM+ Wireless Blood Pressure Monitors because the devices may not meet requirements for systolic pressure.
Megadyne Medical Products is recalling 8,380 MegaPower Electrosurgical Generators because plugging two devices into the same port can activate both, potentially causing patient burns.
Siemens Medical Solutions is recalling 605 Artis Q. angiography systems due to a potential hardware issue that may cause thermal effects and damage to system parts.
Beekley Corporation is recalling S-SPOT REF 777 and 777S markers because they may create imaging artifacts that mimic calcifications on mammograms.
Tosoh Bioscience is recalling 665 HLC-723G8 Automated HPLC Analyzers because Hemoglobin AE (HbAE) interferes with HbA1c results on Version 5.23 software.