State
72,936 recalls have nationwide distribution and so reach Nebraska. 4,547 additional recalls listed Nebraska specifically in their distribution scope.
Of the 4,547 recalls naming Nebraska we have scored against our rubric, 705 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,119 (25%) are Severe.
Which agencies issued them
These figures cover only the 4,547 recalls whose distribution notice names Nebraska specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
About 600 Shintenchi 6-drawer dressers are being recalled because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards to children.
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.
About 2,900 Fixwal 7-Drawer Dressers are being recalled because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards to children.
About 3,500 Cobelae Busy Books for toddlers are being recalled because beads on page eight can loosen and detach, posing a choking hazard.
About 300 Semfri-branded children's multi-purpose helmets are being recalled because they do not comply with the mandatory safety standard for bicycle helmets.
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 795,834 units of Live it Up brand Super Greens because the products may be contaminated with Salmonella Typhimurium.
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.
Weaver's Brew is recalling 421 cases of Goldenroot Lemon Ginger Jalapeno Ginger Beer because the products might contain ginger juice that did not undergo the required pasteurization process.
Philips North America is recalling 6 units of the Upgrade to MR 7700 because exported MR Elastography stiffness maps may show stiffness value errors.
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.
Prima Vera Nueva is recalling 9,656 packages (4 tamales per package) of Roasted Pumpkin & White Cheddar Tamales over potential contamination with Listeria monocytogenes.
Gold Star Distribution is recalling condoms over potential exposure of rodents and rodent activity in its distribution center.
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.
Daimler Coaches is recalling 2026 Mercedes-Benz Tourrider buses because a faulty door valve may prevent doors from opening, delaying emergency evacuation.
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.
Aju Pharm is recalling 200 units of the Genesis Push-In Suture Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.
Siemens is recalling 7 units of the LUMINOS Q.namix T 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 233 units of the Fixone Hybrid Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.
Gold Star Distribution is recalling toothbrushes and toothpaste-with-brush packs over potential exposure of rodents and rodent activity in its distribution center.
Philips North America is recalling 3 units of the SmartPath to dStream for XR and 3.0T because exported MR Elastography stiffness maps may show stiffness value errors.
Aju Pharm is recalling 600 units of the Genesis Screw-In Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.