State
73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Jayco is recalling 2017 Pinnacle Fifth Wheel trailers because the suspension may allow tires to contact the structure, causing damage and increasing crash risk.
Jayco is recalling 2016-2017 Alante motorhomes because a missing heat shield may expose hydraulic lines to excessive heat, increasing the risk of a fire.
Signature Hardware is recalling Luyten Resin Bath Stools because the legs can bend or break during use, posing a fall and injury hazard.
VIQUA is recalling solenoid valve kits for UV water treatment systems because electrical current could leak, posing a shock hazard. No injuries have been reported.
Subaru is recalling 2015-2018 Foresters with heated seats because a loose electrical connection may cause the front passenger airbag to deactivate, increasing injury risk in a crash.
Ridgewood is recalling approximately 1 million Belmont four-drawer dressers sold at Kmart because they can tip over or entrap children if not anchored to the wall.
Darmerica, LLC is recalling 1.8 kilograms of bulk Quinacrine Dihydrochloride API because testing revealed the product was actually Artemisinin.
Johnson Matthey Inc. is recalling 26,625 grams of Cisplatin Active Pharmaceutical Ingredient due to potential glass contamination.
BMW is recalling 2000-2002 323, 325, and 330 models because the driver-side air bag inflator may explode, posing a risk of serious injury or death.
Lamborghini is recalling 441 Aventador S vehicles because engine software may cause the engine to stall when coasting to a stop, increasing crash risk.
Sentinel CH SpA is recalling Alinity c Lithium Reagent Kits due to a potential carryover issue that may result in falsely elevated lithium patient results.
BMW is recalling 416 2020 S1000 RR motorcycles because oil cooler hoses may not be attached properly, potentially causing an oil leak that increases crash risk.
Elekta Inc is recalling 49 Monaco RTP Systems because unintentional changes to electron density settings may cause incorrect dose calculations for radiation therapy plans.
Medline Industries is recalling 500 electric surgical clippers because a defective circuit board component may cause the charger base to overheat and malfunction.
Daimler Vans USA is recalling 2018-2019 Mercedes-Benz and Freightliner Sprinter vans because their airbag systems may not have been activated, increasing crash injury risk.
Daimler Vans USA is recalling 2018-2019 Mercedes-Benz Sprinter and Metris vans because they left the reassembly plant without final quality inspection of safety-relevant parts.
Elekta Inc is recalling 30 units of the Monaco RTP System 5.40 Unity because unintentional changes to electron density settings may result in incorrect dose calculations for radiation treatment plans.
Arrow International Inc is recalling 231 units of 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Kits because they may contain the incorrect banner card.
Cardinal Health is recalling 38 syringes of Nucala (mepolizumab) because the product was stored and shipped outside of labeled temperature requirements.
Sentinel CH SpA is recalling 15,919 MULTIGENT Lithium reagent kits due to a potential carryover issue that may cause falsely elevated patient results.
Johnson Matthey Inc. is recalling Oxaliplatin Active Pharmaceutical Ingredient due to potential glass contamination. The product was distributed nationwide in the United States.
Philips is recalling infant/child defibrillator pads due to incorrect age range labeling on the foil packaging.
Abbott is recalling 159 APS Accelerator modular systems because the safety pacemaker label is missing. The Operations Manual has been updated to specify a 200 mm minimum safety distance for pacemaker wearers.
GE Healthcare is recalling Proteus XR/a radiographic systems because they may fail to provide an audible indication when an exposure is complete.
GN Otometrics is recalling Gold Cup and Snap Leadwires because the electrode lead connector has a protruding conductor beyond the insulation.