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.
Keystone RV is recalling 2017-2019 Dutchmen Voltage and 2019 Endurance travel trailers because tires may contact the rear floor support, affecting handling.
Ford is recalling specific 2010-2014 models because passenger air bag inflators may explode due to humidity, posing a serious injury risk.
Tesla is recalling 2014-2016 Model S vehicles because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.
WSB Inc is recalling SC101 half-helmets manufactured in January 2018 because they may not adequately protect the wearer's head during an impact.
Vantage Mobility International is recalling 2014-2017 AMS Edge II vehicles because a deteriorating fuel pump gasket may cause fuel leaks, increasing fire risk.
Airstream is recalling 2019 Basecamp X recreational vehicles because the tire placard lists incorrect tire sizes and pressure requirements, which could lead to overinflation and increased crash risk.
Takata is recalling certain frontal passenger air bag inflators in 2011 and newer vehicles registered in 22 states and D.C. due to a risk of explosion.
Takata is recalling specific frontal passenger air bag inflators in 2010 or newer vehicles registered in 22 states due to a risk of explosion.
Takata is recalling specific frontal passenger air bag inflators that may explode due to humidity and heat, posing a risk of serious injury or death.
Ford is recalling 2019 EcoSport vehicles because improperly welded front seat frames may cause the seat back to be loose, increasing injury risk in a crash.
Medical Action Industries is recalling 2,600 laparotomy sponges because a breach of the sterile barrier may have compromised product sterility.
Pierce Manufacturing is recalling 2004-2018 aerial vehicles because the aerial device may unexpectedly rotate right during extension, increasing injury risk.
Medtronic is recalling specific MiniMed insulin pump models because software version 4.10 may fail to play expected audio sounds during alerts, alarms, or sirens.
Tosoh Bioscience is voluntarily recalling ST AIA-PACK Testosterone kits due to a Class II defect. The recall covers 26,745 units distributed nationwide.
Radiometer America Inc is recalling 2,131 ABL800 analyzers because software may cause a mismatch between patient demographics and test results.
Tosoh Bioscience Inc is voluntarily recalling AIA-PACK Folate reagents used for in vitro diagnostic testing due to a Class II safety concern.
Tosoh Bioscience Inc is voluntarily recalling ST AIA-PACK FT3 reagents used for in vitro diagnostic testing of Free Triiodothyronine. The recall covers 24,083 units distributed nationwide.
Baxter Healthcare is recalling 123 GEM Coupler Forceps units because of potential rust on the devices. The recall covers nationwide and international distribution.
Howmedica Osteonics Corp. is recalling HydroSet XT Injectable HA Bone Cement because the product displays an incorrect expiry date of 9-Feb-20 instead of the correct 30-Aug-19.
Hologic is recalling 337 I-View Contrast Enhanced Digital Mammography systems due to a calibration issue that prevents visualization of contrast uptake.
Tosoh Bioscience Inc is voluntarily recalling 1,085 units of ST AIA-PACK ACTH in vitro diagnostic reagents distributed nationwide in the US.
Tosoh Bioscience Inc is recalling AIA-PACK B12 reagents because fluorescein interference may cause inaccurately elevated Vitamin B12 test results.
Howmedica Osteonics Corp. is recalling HydroSet XT Injectable HA Bone Cement because the product labels display an incorrect expiry date.
Tosoh Bioscience is recalling 992 units of ST AIA-PACK Homocysteine reagents used for in vitro diagnostic testing. The voluntary recall covers all lots distributed nationwide.
Arcimoto is recalling 2018 FUV motorcycles because incorrect machining of the transmission case may cause premature gearbox failure, potentially immobilizing the vehicle and increasing crash risk.