State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Dunkin' Donuts is recalling approximately 8,300 glass tumblers because they can crack or break, posing laceration and burn hazards.
McLaren is recalling 2012 MP4-12C Spider vehicles because passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.
Toyota is recalling specific 2006-2012 models because passenger air bag inflators may rupture in a crash, potentially sending metal fragments into the cabin.
Altec is recalling 2005-2016 telescoping aerial devices because the winch brake may be improperly oriented, potentially causing unexpected winch line movement and injury.
Heartland is recalling 2017 Mallard recreational trailers because the certification label may contain incorrect tire size or pressure information, which could lead to improper tire inflation or overloading.
USDA FSIS issued a public health alert about ready-to-eat chicken breast strips produced by House of Raeford on Sept. 29, 2016 that may be contaminated with Listeria monocytogenes. No illnesses have been reported.
Karma Automotive is recalling 2012 Fisker Karma vehicles because passenger air bag inflators may rupture during deployment, potentially causing serious injury or death.
Kia is recalling one 2016 Optima because the driver's frontal air bag inflator seal may not be installed properly, potentially reducing inflation in a crash.
GE Healthcare is recalling RFX and other systems because aged CRT monitors may fall. This poses a risk of injury or property damage.
GE Healthcare is recalling ADVANTX LCA and other systems because aged CRT monitors may fall. The recall covers 1,598 units in the US and internationally.
Cargill Cocoa & Chocolate is recalling 50 lb. cartons of Wilbur Semi-Sweet Chocolate Drops because they may contain undeclared milk.
Walt Disney Parks and Resorts is recalling Minnie and Mickey Mouse infant hoodie sweatshirts because the snaps can detach, posing a choking hazard to young children.
GE Healthcare is recalling specific CRT monitors due to a risk that aged units may fall. The recall affects multiple imaging system models.
GE Healthcare is recalling Innova 2000 and other systems because aged CRT monitors may fall. The recall covers 1,598 units in the US and abroad.
GE Healthcare is recalling Prestilix and other systems because aged CRT monitors may fall. The recall covers 1,598 units in the US and overseas.
GE Healthcare is recalling specific X-ray systems because aged CRT monitors may fall. The recall covers 1,598 units distributed in the US and internationally.
GE Healthcare is recalling ADVANTX LCV+ systems because aged CRT monitors may fall. The recall covers 1,598 units distributed in the US and internationally.
GE Healthcare is recalling specific CRT monitors due to the potential for the units to fall. The recall affects multiple system models including ADVANTX and Prestige.
Medtronic Xomed is recalling NIM EMG Endotracheal Tubes because wire in the tubing can become exposed, posing potential harm to intubated patients.
GE Healthcare is recalling Precision 500D and other systems because aged CRT monitors may fall.
Toshiba is expanding a recall of Panasonic lithium-ion battery packs for laptops due to overheating, burn, and fire risks. No injuries have been reported.
GE Healthcare is recalling Prestige II and other systems because aged CRT monitors may fall. The recall covers 1,598 units in the US and abroad.
Kerry, Inc. is recalling 478 bags of Kerry Upgrade Bio WS because the product was identified as being adulterated with Bacillus cereus.
GE Healthcare is recalling Prestige VH and other medical systems because aged CRT monitors may fall.
Curio Design is recalling Splyt modular light kits and bases because cracked pieces and faulty wires pose shock and fire hazards. No injuries have been reported.