State
72,940 recalls have nationwide distribution and so reach Wyoming. 3,219 additional recalls listed Wyoming specifically in their distribution scope.
Of the 3,219 recalls naming Wyoming we have scored against our rubric, 762 (24%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 543 (17%) are Severe.
Which agencies issued them
These figures cover only the 3,219 recalls whose distribution notice names Wyoming specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ford is recalling 2025 F-59 and F-53 vehicles because an incorrectly installed switch may cause brake lights to malfunction, increasing crash risk.
Eureka Inc is recalling 32 cases of ground cinnamon in 100g clear plastic containers over elevated levels of lead.
Boston Scientific is recalling 21 Coyote over-the-wire PTA balloon dilatation catheters over the potential for inflation and deflation difficulty during use in the peripheral vasculature.
Gold Star Distribution is recalling DayQuil Cold and Flu over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Alexis Fire Equipment is recalling two tanker trucks (2022 and 2024) because loose axle clamp fasteners may cause a loss of vehicle control.
Gold Star Distribution is recalling Liquid DayQuil over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Gold Star Distribution is recalling NyQuil Cold and Flu over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Gold Star Distribution is recalling Children's NyQuil Cold & Flu over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Gold Star Distribution is recalling Excedrin over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Philips Medical Systems Nederland is recalling 38 Allura Xper FD10C systems because the drip tray beneath the cooling unit may not have been installed.
Medline is recalling 633 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.
Philips Medical Systems Nederland is recalling 8 units of the Allura Xper FD20/20, model 722038, because the drip tray beneath the cooling unit may not have been installed.
Medtronic is recalling 7,123 units of the Vanta Clinician Programmer Application after complaints that it does not function as intended during use.
Sun Pharmaceutical Industries is recalling 24,624 bottles of Fluocinolone Acetonide Topical Solution 0.01% after an out of specification result for a known impurity.
Medline is recalling 12 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.
Philips Medical Systems Nederland is recalling 56 units of the Allura Xper FD10, model 722010, because the drip tray beneath the cooling unit may not have been installed.
Sun Pharmaceutical Industries is recalling Clindamycin Phosphate Topical Solution 1% after out of specification results for total impurities and for assay.
Philips Medical Systems Nederland is recalling 18 units of the Allura Xper FD20 Biplane, model 722008, because the drip tray beneath the cooling unit may not have been installed.
Philips Medical Systems Nederland is recalling 12 units of the Allura Xper FD10F, model 722002, because the drip tray beneath the cooling unit may not have been installed.
Philips Medical Systems Nederland is recalling 22 units of the Allura Xper FD10/10, model 722027, because the drip tray beneath the cooling unit may not have been installed.
Medline is recalling 5314 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.
Philips Medical Systems Nederland is recalling 10,466 Azurion systems on software versions R2.1.10 and R2.2.10 over six identified software issues including continuous restart.
Heraeus Medical is recalling PALACOS MV+G pro 40 and PALACOS MV+G pro 80 bone cement because an unfortunate combination of factors can leave ampoules unbroken, so no appropriate cement dough is formed.
Philips Medical Systems Nederland is recalling 93 units of the Allura Xper FD10, model 722003, because the drip tray beneath the cooling unit may not have been installed.
Philips Medical Systems Nederland is recalling 14 units of the Allura Xper FD10/10, model 722005, because the drip tray beneath the cooling unit may not have been installed.