State
72,919 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 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Iron-containing dietary supplements from eleven brands are recalled because their packaging is not child-resistant as required by the Poison Prevention Packaging Act. About 356,140 units are affected.
Happiness Light LED lights are recalled because their lithium coin batteries can be accessed easily by children, posing an ingestion hazard. About 2,800 units are affected.
Prestige-branded Supernova and Typhoon butane torch lighters are recalled because they do not have the child-resistant mechanism required by the mandatory lighter standard. About 4,300 units are affected.
Maitys drinkware charms are recalled because they contain loose magnets that violate the mandatory magnet standard, posing an ingestion hazard to children. About 16,400 units are affected.
Muscccm pool drain covers are recalled because they violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act, posing entrapment and drowning hazards.
VEEKTOMX VT103 mini power banks are recalled because the lithium-ion battery can overheat and ignite. Three fires causing minor property damage have been reported; no injuries.
Head ski boots with fluorescent yellow components from model years 2016 through 2022 are recalled because those materials can deteriorate and break, posing a risk of injury from a fall.
Chrysler is recalling 2026 Jeep Wrangler vehicles because insufficient child seat tether welds may reduce restraint effectiveness during a crash.
Akron Brass is recalling Enovation Controls PowerView 700 displays that may fail to power on or respond to touch, preventing the activation of emergency lights and equipment.
SCUBAPRO Monorail Weight Pockets are recalled because the D-ring handle used to release the pocket from a buoyancy compensator can detach, preventing weight ditching in an emergency.
Breez 2-in-1 Smart Bedroom Fan and White Noise Machines are recalled because the internal power connector can corrode and cause the fan to overheat, posing a fire risk.
Male-to-male extension cords sold on Walmart.com are recalled because their exposed prongs can become energized when one end is plugged into a generator, posing an electrocution risk.
Silks-branded children's loungewear sets are recalled because they violate mandatory flammability standards for children's sleepwear. About 7,900 units are affected.
Easymake adult portable bed rails are recalled because users can become entrapped within the rail or between the rail and the mattress, posing a risk of death by asphyxiation.
Chrysler is recalling 2025–2026 RAM 1500, 2500, 3500, 4500, and 5500 vehicles due to a software error that may cause the instrument panel display to fail, hiding critical safety information like gear selection and warning lights.
Philips Respironics is recalling the Trilogy EV300 ventilator because in some situations the Obstruction Alarm does not trigger within the timeframe required by the relevant standards.
Philips Respironics is recalling the Trilogy Evo Universal ventilator because in some situations the Obstruction Alarm does not trigger within the timeframe required by the relevant standards.
Philips Respironics is recalling the Trilogy Evo O2 ventilator because in some situations the Obstruction Alarm does not trigger within the timeframe required by the relevant standards.
One lot of Magnesium Sulfate in Water for Injection is being recalled after a foil pouch labeled as magnesium sulfate was found to contain an IV bag of tranexamic acid.
Imu-Tek Animal Health has recalled Imu-Tek Colostrum-5 Powder because the product may be under-processed. The recalled lot was distributed across 29 states.
Philips Respironics is recalling the Trilogy Evo ventilator because in some situations the Obstruction Alarm does not trigger within the timeframe required by the relevant standards.
Burlington Medical is recalling kilt blockers because of the potential for attenuation degradation over time, decreasing the lifespan of the product.
A further quantity of Prazosin Hydrochloride tablets is being recalled after detection of the nitrosamine impurity N-nitroso-prazosin impurity C above acceptable limits.
Philips is recalling the Azurion 5 M20 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Leader Ultra Lubricating Eye Drops, containing polyethylene glycol 400 and propylene glycol, are being recalled for lack of assurance of sterility.