State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Medical Vision Ab is recalling 3,295 Double Pump RF Patient Cassettes because sterile package breakage may compromise device sterility.
Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.
Terumo is recalling 2,207 cardiovascular procedure kits because they are labeled as containing coated tubing but actually contain non-coated tubing.
Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.
Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.
Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.
Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.
Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.
Honda is recalling 2015 Acura TLX vehicles because transmission wire harness connections may have insufficient crimps, causing the vehicle to unexpectedly shift to neutral and increasing crash risk.
Volkswagen Group of America is recalling 2017 Audi Q7 vehicles because the third-row seat back may move forward in a crash, increasing injury risk.
Ford is recalling specific 2012-2016 vehicles because door latches may break, allowing doors to open while driving.
Mazda is recalling specific 2010-2016 models because lift gate support struts may corrode and break, causing the gate to drop unexpectedly and injure users.
Volkswagen Group of America is recalling certain Audi models because software may cause side marker lights to fail, reducing visibility at night.
Nissan is recalling certain 2015-2017 Maxima and Murano vehicles because brake fluid may leak onto an electrical circuit board, increasing the risk of a fire.
Tiffin is recalling 2017 Allegro Bus motorhomes because the passenger side mirror may move while driving, reducing visibility and increasing crash risk.
Spartan Motors is recalling 151 model year 2016 Utilimaster Walk-In Vans because the driver's seat may recline unexpectedly, increasing crash risk.
John Deere is recalling about 50 model 485A backhoe attachments because mounting hardware could loosen, causing the frame to rotate and crush the operator.
Kaufman Trailers is recalling 285 model year 2015-2016 Mini 5-Car Haulers because a suspension spring eye may break, allowing the axle to slide and increasing crash risk.
Polaris is recalling approximately 13,000 RZR XP Turbo recreational off-highway vehicles because engine overheating and loose drain tubes can cause fires and severe burn injuries.
Goodyear is recalling specific G399A LHS tires due to a manufacturing defect that may cause tread separation, increasing the risk of a crash.
SAHN Designs is recalling SAHN Classic SH523 bicycle helmets because they do not meet federal impact safety standards, posing a risk of head injury.
KTM North America is recalling about 920 model year 2016 KTM and Husqvarna motocross motorcycles because a connecting rod can fracture, causing a crash.
Alere San Diego is voluntarily recalling INRatio2 PT/INR Home Monitoring Systems because they may display inaccurate INR results compared to central laboratory tests.
Cook Inc. is recalling Slip-Cath Beacon Tip Catheters because polymer degradation can cause the tip to fracture or separate, potentially leading to device fragments in the body.
Conmed is recalling Pediatric ThermoGard Dual Dispersive Electrodes because they may be incompatible with some electrosurgical generators, posing a risk of undetected pad lift and potential burns.