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.
4 C Foods, Corp. is recalling Cento Parmesan Grated Cheese because FDA samples revealed Salmonella contamination. Consumers should stop using the product.
North American Rescue LLC is recalling Mini Resupply Trauma Kits because the manufacturer has concerns about the sterility of the included eye wash solution.
Chocolate Shoppe Ice Cream Co. is recalling Peanut Butter Cookie Dough Ice Cream because the cookie dough pieces may be contaminated with Listeria monocytogenes.
Centurion Medical Products is recalling 1,000 Multi-Med Single Lumen Catheter kits because excess material at the catheter tip may separate and cause an embolism.
North American Rescue LLC is recalling Advance Trauma Kits because the manufacturer has concerns regarding the sterility of the eye wash irrigating solution.
Thayer Intellectual Property, Inc. is recalling 339 MANOS EX surgical devices because customers were not notified of a critical safety warning regarding device bending and breakage.
Mondelez Global LLC is recalling Oreo Fudge Creme cookies (Original and Mint varieties) because milk is not declared on the ingredient list.
Saputo Cheese USA is recalling 558 lbs of Italian White Trim cheese after a food service customer reported finding white plastic in the product.
3M is recalling Universal Electrosurgical Pads because an unintended process liner may impede the safe return of electrosurgical current, increasing the risk of patient burns.
North American Rescue LLC is recalling K-9 Trauma Field Kits because the manufacturer has concerns about the sterility of the included eye wash irrigating solution.
Mercedes-Benz is recalling 2014 CLA250 vehicles because a brake booster fitting may break, increasing the force needed to apply brakes and raising crash risk.
Mercedes-Benz is recalling certain 2015-2016 models because axle bolts may not have been assembled correctly, potentially fracturing and causing vehicle instability.
North American Rescue is recalling Amphibious Trauma Kits because the manufacturer has concerns about the sterility of the eye wash solution.
North American Rescue LLC is recalling Range Trauma Kit Hardcases because the manufacturer has concerns about the sterility of the eye wash irrigating solution included in the kits.
Calbee North America is recalling one lot of black pepper flavored green pea crisps because they may contain undeclared milk.
Mercedes-Benz is recalling specific 2013-2016 models because a steering control unit defect may cause loss of power steering assist or a fire.
North American Rescue LLC is recalling USCG Boat Response Kits because the manufacturer has concerns about the sterility of the eye wash irrigating solution.
Mondelez is recalling Oreo Fudge Creme cookies because milk is not listed on the ingredient label.
North American Rescue LLC is recalling Aid Backpack Kits because the manufacturer has concerns about the sterility of the eye wash irrigating solution.
Triple E is recalling 18 model year 2017 Serenity S24CB recreational vehicles because an incorrectly connected circuit wire poses a fire risk.
KZRV is recalling 2016-2017 Durango and Venom trailers because rear cargo door hinges may have insufficient welds, causing the door to swing down with excessive force.
North American Rescue is recalling specific Range Trauma Kits because the manufacturer has concerns about the sterility of the included eye wash solution.
To Your Heart's Content is recalling Plush Puffs Marshmallows in Toasty Coconut flavor because the product contains undeclared milk.
MORryde is recalling approximately 2,500 Zero G Ramp Door hinges manufactured between August 21, 2016, and December 12, 2016, because insufficient welds may cause the door to swing down with excessive force.
Merge Healthcare is recalling eFilm Workstation software versions 2.1 through 4.1 because RF projection images may display incorrect measurements without a calibration indicator.