State
73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Garia is recalling about 1,000 battery-powered golf and courtesy vehicles because a fuse can overheat and melt while charging, posing a fire hazard.
John Deere is recalling 60-inch broom attachment kits for compact utility tractors because they lack the required Operator's Manual, posing an injury hazard.
Aromatics International is recalling Wintergreen Essential Oil because the packaging is not child-resistant, posing a risk of poisoning to young children.
W8 Distributing is recalling Jade Bloom Wintergreen and Birch Sweet Essential Oils because the packaging is not child-resistant, posing a poisoning risk to young children.
Flybar is recalling Swurfer Kiwi Baby and Toddler Swings because a plastic stopper can detach, posing a fall hazard to the occupant.
Heartland is recalling 2020 Trail Runner, Wilderness, Mallard, and Prowler trailers because a U-bolt on the spare tire carrier may break, causing the tire to detach.
Organic Pure Oil is recalling Wintergreen Essential Oil because the packaging is not child-resistant, posing a risk of poisoning to young children.
Sterno Home is recalling Hampton Bay, Patriot, and Paradise path light kits because a defective power supply poses an electric shock risk.
Applied Medical Resources Corp is recalling Bard Embolectomy Catheters because the tips may separate during use, posing a risk of dislodgement in patients.
Applied Medical Resources Corp is recalling Python Embolectomy Catheters because the tips may separate during use, posing a risk of unintended dislodgement in patients.
Philips Ultrasound Inc is recalling S7-3t transesophageal transducers because a programming error prevents the system from measuring tip temperature, which may stop auto-cooling and cause patient injury.
Medifast is recalling Optavia Old Fashioned Maple & Brown Sugar Oatmeal pouches because they contain undeclared milk.
Royal International Trading Inc. is recalling Tainy Boctoka Dry Fruits Mix because the product contains undeclared sulfites.
Philips Ultrasound Inc is recalling S8-3t transesophageal transducers that may fail to measure tip temperature correctly, potentially preventing auto-cooling and causing patient injury.
ICU Medical is recalling 675 IV administration sets that may contain a 15 drops/mL cannula instead of a 10 drops/mL cannula, risking under-delivery of critical medication.
Maquet Cardiovascular is recalling Hemashield Platinum vascular grafts due to potential small holes at seam lines that could cause intra-operative bleeding.
ICU Medical is recalling 50 units of 10 Drop Primary IV Sets because they may contain 15 drops/mL cannulas, risking under-delivery of critical medications.
LiquidSpring is recalling specific suspension systems for 2019-2020 RAM 4500 and 5500 vehicles because the rear brake line may wear, causing brake failure.
Applied Medical Resources Corp is recalling 28,799 Dual Lumen Graft Cleaning Catheters due to reports of tip separation during use, which may expose patients to unintended dislodgement.
ICU Medical is recalling veterinary IV administration sets that may contain a 15 drops/mL cannula instead of 10 drops/mL, risking under-delivery of medication.
ICU Medical is recalling IV administration sets that may contain a 15 drops/mL cannula instead of 10 drops/mL, risking under-delivery of critical medication.
ICU Medical is recalling 14,000 IV administration sets that may contain a 15 drops/mL cannula instead of 10 drops/mL, risking under-delivery of critical medication.
Volkswagen Group of America is recalling 2020 Audi A6, A7, and Allroad vehicles because the passenger airbag may not deploy properly, increasing injury risk.
Maquet Cardiovascular is recalling specific Hemashield Platinum vascular grafts due to potential small holes at seam lines that could cause intra-operative bleeding.
Porsche is recalling 2,253 Cayenne vehicles because a fuel line connector may leak, increasing the risk of fire.