State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Akron Brass Company is recalling Ultrajet firefighting nozzles because internal components may bind, limiting water output and hindering firefighting efforts.
Segway is recalling specific off-board chargers for Personal Transporters because a wire can detach and cause a shock hazard. No injuries have been reported.
KZRV is recalling 2018 Sport Trek and Durango travel trailers with outside kitchens due to potential propane line leaks that could cause fire or explosion.
Marcho Farms is recalling approximately 5,620 pounds of veal, beef, and pork products due to possible non-O157 Shiga toxin-producing E. coli contamination.
Combi USA is recalling about 1,000 Shuttle Travel Systems because the car seat can disengage from the stroller frame, posing a fall hazard to infants.
Honda is recalling 2015-2016 CR-Vs that received replacement engines potentially built with wrong pistons, which may cause engine stalls and increase crash risk.
Jim Reed's Truck Sales is recalling 2014-2016 Hino 338 trucks because certification labels fail to identify the final stage manufacturer, potentially hindering safety recall awareness.
Deutsch Kase Haus, LLC is recalling approximately 4.1 million pounds of Colby cheese due to potential Listeria monocytogenes contamination. The product was distributed in 11 states.
Deutsch Kase Haus, LLC is recalling Amish Creamery cheese products due to potential Listeria monocytogenes contamination. The recall affects multiple private-label brands distributed across eleven states.
Deutsch Kase Haus, LLC is recalling approximately 4.1 million pounds of Colby-Jack cheese due to potential Listeria monocytogenes contamination. The product was distributed to 11 states.
Deutsch Kase Haus, LLC is recalling bulk liquid whey due to potential Listeria monocytogenes contamination. The product was distributed to multiple states.
Deutsch Kase Haus is recalling cheddar cheese products due to potential Listeria monocytogenes contamination. Affected brands include Guggisberg, Amish Classics, Dutch Farms, and Banquet.
Deutsch Kase Haus, LLC is recalling White Colby cheese due to potential Listeria monocytogenes contamination. The product was distributed in 11 states.
Deutsch Kase Haus, LLC is recalling specific cheese by-products due to potential Listeria monocytogenes contamination. The products were distributed across eleven states.
Deutsch Kase Haus, LLC is recalling bulk cream due to potential Listeria monocytogenes contamination. The product was distributed to multiple states.
Deutsch Kase Haus is recalling Colby-Jack cheese products due to potential Listeria monocytogenes contamination. The recall affects private-label brands sold in 11 states.
Deutsch Kase Haus is recalling private-label farmers cheese due to potential Listeria monocytogenes contamination. Affected products were distributed in 11 states.
Deutsch Kase Haus, LLC is recalling Pepper-Jack cheese due to potential Listeria monocytogenes contamination. The product was sold under multiple private labels in 11 states.
Deutsch Kase Haus, LLC is recalling specific lots of semi-soft cheese due to potential Listeria monocytogenes contamination. The affected products were distributed to multiple states.
Isomeric Pharmacy Solution, LLC is recalling 5,165 bottles of Phenylephrine 2.5% and Tropicamide 1% ophthalmic drops due to a lack of assurance of sterility.
Isomeric Pharmacy Solution, LLC is recalling 2,335 vials of Triamcinolone Acetonide and Lidocaine HCl injection due to production processes that cannot assure sterility.
The FDA is recalling hCG Body Shaper because it was marketed without approval and contains human chorionic gonadotropin, making it an unapproved drug.
Medtronic is notifying clinicians that an improved splice kit is available to replace the HeartWare HVAD Pump Driveline Splice Kit due to a safety issue.
Volkswagen Group of America is recalling 2017 Audi Q5 vehicles because a gearbox defect may allow the vehicle to roll unexpectedly while in Park.
Porsche is recalling 2015-2017 Macan models because a fuel pump flange may crack, causing a fuel leak that increases fire risk.