State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Rosenbauer is recalling 2015 Commander fire trucks because improperly tightened axle nuts could cause the driveshaft to disconnect, increasing crash risk.
Rosenbauer is recalling 2014-2015 Commander fire trucks because loose ball joints in certain front suspension assemblies could separate, causing a loss of steering control.
Winnebago is recalling 2015-2016 Travato, Trend, and Itasca Viva! motorhomes because an ignition switch defect may cause the vehicle to stall or disable safety systems.
Vanguard is recalling 2014-2015 Dry Freight Van Trailers because improperly seated brake diaphragms may cause drag, potentially leading to wheel end fires.
Meritor is recalling certain trailer axle assemblies equipped with specific air brake actuators that may experience brake drag, posing a risk of wheel end fire.
Britax is recalling about 71,000 B-Safe 35 infant car seats because the carry handle can crack and break, posing a fall hazard to infants.
Chillafish is recalling BMXie, Jack, and Josie balance bikes because overinflated tires can cause plastic rims to crack and send pieces flying, posing a laceration hazard.
Britax is recalling B-Ready strollers and replacement top seats because foam padding on the arm bar can break off, posing a choking hazard to children.
Snapp's Ferry Packing Company is recalling approximately 410 pounds of ground beef that may be contaminated with E. coli O157:H7.
Nestle Waters North America is recalling Sweet Leaf Organic Half and Half Lemonade Tea because the product contains glass particles.
Motor Coach Industries is recalling specific MCI buses because missing welds on driver seat brackets could allow seat belt anchors to separate, increasing injury risk in a crash.
Ortho-Clinical Diagnostics is recalling VITROS 5600 Chemistry Systems due to a software anomaly that may cause erroneous test results without user notification.
Nestle Waters North America is recalling Sweet Leaf Organic Original Sweet Tea because the product contains glass particles.
CompView Medical is recalling 10 NuCARTGN mobile display units because the spring arm may detach if the securing ring was not installed correctly.
Altec is recalling 2010-2015 AH75, AH85, and AH100 aerial devices because a hydraulic valve may allow unexpected movement, increasing injury risk.
Zimmer Biomet is recalling the Virage OCT Spinal Fixation System because set screw staking is out of specification, which can interfere with rod insertion.
Cheryl & Co. is recalling Jingle Bell ornaments sold by QVC because sharp metal edges on the cutouts pose a laceration hazard.
Nestle Waters North America is recalling Sweet Leaf Organic Tea Mint & Honey because the product contains glass particles.
OrthoPediatrics Corp is recalling 102 Response Spine UniAxial Pedicle Screws because they may have been manufactured incorrectly, preventing the driver from fully engaging the screw.
Nestle Waters North America is recalling Sweet Leaf All Natural Peach Iced Tea because the product contains glass particles.
Brainlab AG is recalling RT Elements software because large objects may display cropped during import, potentially affecting radiation treatment planning.
Ortho-Clinical Diagnostics is recalling VITROS 3600 Chemistry Systems due to a software anomaly that may allow the device to process assays at incorrect temperatures, potentially producing erroneous results.
Intuitive Surgical is correcting the da Vinci Xi I&A User Manual to prevent unintended patient harm from capacitive coupling when using 8mm endoscopes with specific instruments.
GMAX Helmet LLC is recalling specific GM78 Fullface helmets that may not adequately protect users in a crash. Owners can exchange the helmet or receive a refund.
Intuitive Surgical is correcting the da Vinci Xi I&A User Manual to warn about unintended patient harm from capacitive coupling when using 8 mm endoscopes with specific instruments.