State
73,737 recalls have nationwide distribution and so reach Utah. 4,914 additional recalls listed Utah specifically in their distribution scope.
Of the 4,914 recalls naming Utah we have scored against our rubric, 524 (11%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,350 (27%) are Severe.
Which agencies issued them
These figures cover only the 4,914 recalls whose distribution notice names Utah specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Chrysler is recalling 319,610 vehicles because a software error can cause the rearview camera image to remain displayed after shifting out of reverse, increasing crash risk.
AAA Cosmetica is recalling bio aaa Advance Hand Sanitizer because it contains methanol. Consumers should stop using the product.
Mylan Institutional LLC is recalling Amiodarone Hydrochloride Injection due to a labeling error where cartons may contain the wrong medication.
Mylan Institutional LLC is recalling 1,407 cartons of Tranexamic Acid Injection due to a labeling error that may result in the wrong medication being dispensed.
SG24 LLC is recalling Skin Guard 24 hand sanitizing towelettes because they contain unapproved methanol and lack FDA approval.
Whole Foods Market is recalling Artequeso Manchego cheese due to undeclared lysozyme from egg whites, a common allergen.
Whole Foods Market is recalling Piave Vecchio cheese nationwide due to undeclared egg whites (lysozyme). Consumers with egg allergies should not consume the product.
Whole Foods Market is recalling Mitica La Dama Sagrada Raw Milk cheese because it contains undeclared lysozyme from egg whites.
Whole Foods Market is recalling specific sliced cheese products because they contain undeclared lysozyme from egg whites, posing a risk to individuals with egg allergies.
SG24 LLC is recalling SkinGuard 24 All-Day Hand Sanitizer because it is an unapproved new drug containing methanol.
Roqueplast is recalling Command Brands GelAnti Bac hand sanitizer due to potential contamination with undeclared methanol.
Whole Foods Market is recalling Forteto Genovese Pesto cheese nationwide due to undeclared egg whites (lysozyme). Consumers with egg allergies should not eat the product.
Whole Foods Market is recalling sliced Mitica Mahon cheese nationwide due to undeclared lysozyme from egg whites, posing a risk to individuals with egg allergies.
SG24 LLC is recalling Skin Guard 24 All-Day Hand Sanitizer pens because they are labeled to contain methanol, making them unapproved new drugs.
SG24 LLC is recalling SkinGuard 24 Hand Sanitizer because it is an unapproved new drug containing methanol.
Whole Foods Market is recalling specific sliced cheeses due to undeclared lysozyme from egg whites, posing a risk to individuals with egg allergies.
E-One is recalling 2018-2020 Typhoon and Cyclone II ambulances because a bracket defect may cause the rear axle to become unsecured, increasing crash risk.
Whole Foods Market is recalling La Marquesa Herb Manchego Raw Milk cheese because it contains undeclared egg whites (lysozyme).
Jayco is recalling 2019-2020 Entegra Reatta, Jayco Embark, and Entegra ReattaXL motorhomes because a damaged circuit board could increase the risk of a fire.
Whole Foods Market is recalling Chimay Biere cheese due to undeclared egg whites. The product was sold nationwide with sell-by dates until September 11, 2020.
Jayco is recalling specific 2016-2019 motorhomes because leveling system brackets may fail, causing components to contact the ground and increasing crash risk.
Horizon Global is recalling specific U-Haul, Draw-Tite, and Reese Towpower trailer hitches sold between November 2019 and August 2020 due to a defect that may prevent the pintle hook from locking securely.
Siemens Healthcare Diagnostics is recalling Dimension Vista High Sensitivity Troponin I reagent cartridges because they may exhibit a negative bias with patient samples.
WHILL is recalling about 1,160 Model Ci personal electric vehicles because a control pad malfunction can cause unintended power changes and speed fluctuations, posing crash and injury hazards.
Siemens is recalling 110 Sensis Vibe Hemo systems because a connector may break, potentially causing the device to stop functioning and lose vital signs.