State
73,722 recalls have nationwide distribution and so reach Minnesota. 7,849 additional recalls listed Minnesota specifically in their distribution scope.
Of the 7,849 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 2,245 (29%) are Severe.
Which agencies issued them
These figures cover only the 7,849 recalls whose distribution notice names Minnesota specifically. The 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Steris Corporation is recalling Vis-U-All High Temperature Tubing because purple ink on the exterior label may bleed during steam processing, causing cosmetic defects and potential ink transfer to devices.
Steris Corporation is recalling Vis-U-All High Temp Self Seal Pouches because purple ink on the exterior label may bleed during steam processing, causing cosmetic defects or ink transfer to devices.
Steris Corporation is recalling Vis-U-All High Temp Self Seal Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to devices.
Steris Corporation is recalling Vis-U-All High Temp Self Seal Pouches because purple ink on the exterior label may bleed during steam processing.
Steris Corporation is recalling Vis-U-All High Temp Heat Seal Pouches because purple ink on the exterior label may bleed during steam processing.
Steris Corporation is recalling Vis-U-All High Temp Self Seal Pouches because purple ink on the exterior label may bleed during steam processing.
Steris Corporation is recalling Vis-U-All High Temp Self Seal Pouches because purple ink on the exterior label may bleed during steam processing, causing cosmetic defects and potential ink transfer to devices.
Steris Corporation is recalling Vis-U-All High Temperature Tubing because purple ink on the exterior label may bleed during steam processing, causing cosmetic defects and potential ink transfer to devices inside the pouch.
Ningbo is recalling Hikari LED headlight bulbs sold on Amazon because they create excessive glare for oncoming traffic, increasing crash risk.
Smeal is recalling 2020 Aerial and Pumper vehicles because a wireless remote controller defect may cause batteries to discharge faster, potentially hindering firefighting efforts.
Strategic Sports is recalling 3,752 Simpson Shorty OTW helmets that lack proper retention and protection, increasing crash injury risk.
PACCAR is recalling 2015-2021 Peterbilt 320 and 520 trucks because the steering column support may crack, increasing crash risk.
Braun Ambulances is recalling specific Crestline CCL150 ambulances because defective seat belt fasteners may fail, increasing injury risk in a crash.
Marion Body Works is recalling one 2018 Freightliner M2-106 vehicle because a license plate light may be aimed at other drivers, increasing crash risk.
Volvo is recalling 2021 V60, V90, XC60, and XC90 models because the SRS control unit may detach during a crash, reducing occupant protection.
Noble House Home Furnishings is recalling four models of chests, cabinets, and dressers because they are unstable and can tip over, posing serious hazards to children.
John Deere is recalling Frontier rotary tillers because some lack a safety sign warning of entanglement hazards. No injuries have been reported.
Automann is recalling Warning Triangle Sets because their color, reflectivity, and stability may reduce effectiveness, potentially increasing crash risk.
USDA FSIS issued a public health alert for HyVee Chicken Enchiladas due to misbranding and an undeclared soy allergen. Consumers with soy allergies should discard the product.
WishGarden Herbs is recalling 298 jars of Goldenseal Powder because testing found Cronobacter Sakazakii contamination.
Wishgarden Herbs is recalling 46 jars of Happy Ducts Compress because the product tested positive for Cronobacter Sakazakii.
Imprimis NJOF, LLC is recalling 6,520 vials of Dexamethasone-Moxifloxacin PF Injection because 13 vials were found with faulty crimps, raising concerns about sterility.
The FDA is recalling specific lots of Covidien TA Auto Suture Vascular Staplers because a damaged internal component may prevent adequate hemostasis or cause tissue damage.
Becton Dickinson & Co. is recalling BD Phoenix PMIC-110 IVDs due to false resistant SXT results with S. aureus, which could impact antibiotic treatment.
Massimo Motor Sports is recalling percussion massage guns sold at Costco because the lithium-ion battery can overheat and cause fires.