State
72,940 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 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
About 4,520 Cumbor retractable safety gates are being recalled because a child's torso can fit through the opening between the gate and the floor.
About 1,600 Vndueey Magnetic Men toy sets are being recalled because they contain magnets that can be swallowed by children. CPSC reports no injuries or incidents.
About 340 Gagaku ice cream shop toy playsets are being recalled because they contain magnets that can be swallowed by children. CPSC reports no injuries or incidents.
About 9,300 Based Online Fidget Magnet Ball Toy Sets are being recalled because they contain magnets that can be swallowed by children. CPSC reports no injuries or incidents.
Blue Bird is recalling 2026-2027 Vision and All American school buses because side and rear windows may have illegible DOT markings, failing federal safety standards.
Blue Bird is recalling one 2026 Vision transit bus because side or rear windows may have illegible DOT markings, failing federal safety standards.
Abbott Diabetes Care is recalling 1,663,241 FreeStyle Libre 3 Plus sensors, REF 78768-01, because carbon build up in the sensor may result in incorrect low glucose results.
One Roof LLC is recalling 197 Atwater's Holiday Cookie Tins over undeclared tree nut allergens: almonds, pecans and walnuts.
Abbott Diabetes Care is recalling 258,913 FreeStyle Libre 3 Plus sensors, REF 78769-01, because carbon build up in the sensor may result in incorrect low glucose results.
Herbs Forever is recalling 45 units of HerbsForever Gastro Care Ayurvedic Herbal Supplement over a potential undeclared allergen, wheat. The FDA has classified the action as Class I.
Abbott Diabetes Care is recalling 1,060,723 FreeStyle Libre 3 sensors because a manufacturing process issue may cause carbon build up that results in incorrect low glucose results.
Abbott Diabetes Care is recalling 8,062 FreeStyle Libre 3 Plus sensors because a manufacturing process issue may cause carbon build up that results in incorrect low glucose results.
Herbs Forever is recalling 45 units of HerbsForever Hingwastika Churna Ayurvedic Herbal Supplement over a potential undeclared allergen, wheat. The action is Class I.
Volkswagen is recalling certain 2023-2024 ID.4 vehicles because the high voltage battery cell modules may contain misaligned electrodes that can result in a battery fire.
Ford is recalling 2026 Explorer vehicles because the windshield may not be properly bonded, posing an injury risk in a crash.
Oshkosh is recalling 230 2025 NGDV and NGDV Electric vehicles because rear axle hub fasteners may loosen, potentially causing the wheel to detach.
Gold Star Distribution is recalling Alka Seltzer over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Gold Star Distribution is recalling Claritin over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Gold Star Distribution is recalling Tylenol 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.
GE Medical Systems Israel is recalling 38 MAXXUS systems because units past end of guaranteed service may have been moved without adequate detector support, risking a detector fall.
ICU Medical is recalling 423 Plum Duo Infusion Systems after one lot of defective primary speakers may fail to produce sound, so the pump may not produce audible alarms or alerts.
GE HealthCare is recalling 12 units of the SMV BodyTrack nuclear medicine system, because systems moved without adequate detector support may suffer a detector fall.
Canon Medical Systems is recalling 22 Vantage Titan 3T MRI systems because ice in the magnet venting system could lead to a helium vessel rupture during a quench.
Gold Star Distribution is recalling Petroleum jelly over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.