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.
About 620 items of Lola + The Boys hooded clothing with drawstrings are being recalled because the drawstrings can catch on objects, posing a strangulation hazard to children.
About 250 Dresbe LED Christmas Headbands are being recalled because children can easily access the button cell batteries and the product lacks the warnings required by Reese's Law.
About 2,970 bottles of GM Gumili Wintergreen Essential Oil are being recalled because the methyl salicylate they contain is not in child-resistant packaging.
Hyundai is recalling certain 2025-2026 IONIQ 5 and 2026 IONIQ 9 vehicles because the high voltage battery system may contain an improperly tightened bus bar, which can cause a short circuit.
About 3,500 Cobelae Busy Books for toddlers are being recalled because beads on page eight can loosen and detach, posing a choking hazard.
Superfoods, Inc. is recalling 795,834 units of Live it Up brand Super Greens because the products may be contaminated with Salmonella Typhimurium.
SunMed Holdings is recalling 89 units of the Filled Broselow Organizer, model 7730IALS, because the product contains potentially harmful dosing errors for Vecuronium, Flumazenil and Ketamine.
SunMed Holdings is recalling 95,300 units of the Broselow Pediatric Emergency Rainbow Tape because the product contains potentially harmful dosing errors for Vecuronium, Flumazenil and Ketamine.
Superfoods, Inc. is recalling Live it Up brand Super Greens powder, net weight 8.5oz, because the products may be contaminated with Salmonella Typhimurium.
SunMed Holdings is recalling 20,583 units of the Broselow Pediatric Emergency Rainbow Tape, model 7700RE, because it contains potentially harmful dosing errors for Vecuronium, Flumazenil and Ketamine.
Fontaine Modification is recalling certain 2024-2025 Freightliner Business Class M2 vehicles because the steering gearbox assembly may have been assembled with insufficient oil.
About 700 Scepter B62 gas and oil combination fuel containers are being recalled because they lack flame mitigation devices and the spout is not child-resistant.
Weaver's Brew is recalling 1,014 cases of Goldenroot Lemon Ginger Hibiscus Ginger Beer because the products might contain ginger juice that did not undergo the required pasteurization process.
Bharat Bazar is recalling 180 packages of Soma Kitchen Natural Asafoetida over undeclared wheat.
Gold Star Distribution is recalling condoms over potential exposure of rodents and rodent activity in its distribution center.
Aju Pharm is recalling 1,088 units of the Fixone Biocomposite Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.
Greenstone is recalling 3,456 cartons of methylprednisolone tablets Dosepak, 4 mg, because the blister foil was applied in the wrong orientation, giving incorrect dosing information.
Siemens is recalling 41 units of the LUMINOS Q.namix R fluoroscopic X-ray system because ortho images may not be flipped as preset and an image of a previous patient may be processed.
Aju Pharm is recalling 416 units of the AlternatiV+ Screw-In Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.
Philips North America is recalling 21 units of the Ingenia Ambition X because exported MR Elastography stiffness maps may show stiffness value errors.
Philips North America is recalling 6 units of the Ingenia 3.0T CX MR system because exported MR Elastography stiffness maps may show stiffness value errors.
Aju Pharm is recalling 400 units of the Genesis Dual Thread Screw-In Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.
Philips North America is recalling 3 units of the Evolution Upgrade 1.5T MR system because exported MR Elastography stiffness maps may show stiffness value errors.
Baxter Healthcare is recalling 125,496 bottles of Sterile Water for Irrigation, 250 mL, after plastic particles from the bottle rim were observed floating in the solution.
Philips North America is recalling 6 units of the Upgrade to MR 7700 because exported MR Elastography stiffness maps may show stiffness value errors.