State
73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Altec is recalling 2018-2020 digger derricks and aerial devices because a hydraulic check valve snap ring can fail, causing unintended boom movement.
Honda is recalling 2002-2006 CR-V vehicles because moisture in the driver-side power window switch may cause it to overheat, smoke, or catch fire.
Honda is recalling 2013-2015 Accord vehicles with 4-cylinder engines and CVTs in 23 states and D.C. because a lubricant issue may cause drive shafts to break, risking loss of power or vehicle roll-away.
Thermo Tents is recalling Mór Series tents because they are incorrectly labeled as fire retardant, posing a fire hazard.
Scentsy is recalling Luminary Jack and Bless This Home electrical oil warmers because corrosion of electrical components poses a fire hazard.
Forest River is recalling 2018-2020 R-POD travel trailers because the sewer termination bracket may fail, causing plumbing to drag or detach and creating a road hazard.
Subaru is recalling 2020 Outback and Legacy vehicles because a software update may cause the rearview display to shut off intermittently, increasing crash risk.
Homfa HPB-087 and HPB-106 cabinets are recalled because they can tip over or entrap children if not anchored to the wall.
Honda is recalling 2018-2020 Accord and 2019-2020 Insight vehicles because a software error may cause system malfunctions that increase crash risk.
Spartan Fire is recalling 2019-2021 Gladiator and MetroStar vehicles because LCD displays may lock up, potentially delaying emergency operations.
Dole Fresh Vegetables Inc. is recalling specific lots of Organic Romaine Hearts because pathogenic non-O157 E. coli STEC was found during routine sampling.
MPM Medical LLC is recalling REGENECARE HA topical anesthetic hydrogel because it was found to be contaminated with Burkholderia cepacia bacteria.
Invacare is recalling 384,767 PerfectO2 V oxygen concentrators worldwide due to a defect that may cause self-extinguishing fires or cap explosions.
CME America is recalling 4,182 NeoThrive syringe pumps because motor wear may cause under-infusion without alarms, and cleaning fluids may damage hardware.
Medtronic is recalling MiniMed 640G insulin pumps because a missing solder battery connection could interrupt power. The recall covers specific serial numbers distributed in the U.S. and abroad.
Audi is recalling 2,355 2018-2019 RS 5 Coupe vehicles because an incorrect positive battery terminal cover could prevent doors from opening or hazard lights from working after a rear crash.
CME America is recalling T34L PCA syringe pumps because motor wear may cause under-infusion without alarms, and cleaning fluids may damage hardware.
Torrent Pharma Inc. is recalling 2,496 bottles of Anagrelide Capsules, USP 1 mg, because the product failed to meet dissolution specifications.
Medtronic is recalling 391 MiniMed 670G insulin pumps because a missing solder battery connection could interrupt power to the device.
L G Sourcing is recalling allen + roth 62-inch electric fireplaces sold at Lowe's because wiring connectors can overheat, posing a fire hazard.
Olympus is recalling ultrasound endoscopes to update cleaning instructions and reduce the risk of patient infections.
Olympus is recalling ultrasound endoscopes to update cleaning instructions and reduce the risk of patient infections.
Verathon is recalling 398 BladderScan Prime Plus Probes because a change in handle material and process may cause the handle to crack.
CME America is recalling T-Syringe Pumps because motor wear may cause silent under-infusion and cleaning fluids may crack hardware.
VEO Diagnostics is recalling 15 ACCEL ELISA COVID-19 antibody test kits because the FDA removed their Emergency Use Authorization. Users should stop using the kits.