State
73,722 recalls have nationwide distribution and so reach Nebraska. 4,580 additional recalls listed Nebraska specifically in their distribution scope.
Of the 4,580 recalls naming Nebraska we have scored against our rubric, 713 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,345 (29%) are Severe.
Which agencies issued them
These figures cover only the 4,580 recalls whose distribution notice names Nebraska specifically. The 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Curt Manufacturing is recalling Rambler RV Towbars because the axial pivot pin may loosen or fail, potentially causing the hitch to separate and increasing crash risk.
Gulf Stream is recalling 2020-2021 Super-Lite 19RD travel trailers because the rear axle may contact the black water tank, causing spills and crash risks.
Mitsubishi is recalling 2014-2019 Outlander and 2018-2019 Outlander PHEV vehicles because the second-row center seat belt buckle may interfere with the right-side buckle, rendering it inoperable.
Forest River is recalling specific 2021 Riverstone trailers equipped with an optional generator prep package due to incorrect transfer switch wiring that may cause voltage back feed.
Altec is recalling 2017-2020 aerial devices due to a power take-off that may leak oil onto the exhaust heat shield, increasing fire risk.
RH is recalling Riveted Mesh Floor Lamps because the foot switch can overheat or catch fire. Consumers should stop using the lamps and contact RH for a refund.
Ananda Apothecary is recalling four essential oil products because their packaging is not child-resistant, posing a risk of poisoning if swallowed by young children.
Miracle Botanicals is recalling Wintergreen and Birch Essential Oils because the packaging is not child-resistant, posing a risk of poisoning if swallowed by young children.
Cooper Lighting is recalling about 39,000 All Field and Prism RGBA light fixtures because lenses can loosen and fall, posing an injury risk to people below.
DaVinci is recalling about 3,000 Bailey bassinets because the mattress support can disengage, posing fall and entrapment risks to infants.
Beyond Better Foods is recalling Enlightened Dairy-Free Chocolate Peanut Butter Frozen Dessert because it may contain undeclared milk.
Mount Franklin Foods is recalling 7-Select Yogurt Pretzels because they may contain undeclared peanuts. The product was distributed to 7-11 stores nationwide.
Beaming White LLC is recalling Koala Hand Sanitizer because the ethanol content is below the label claim and undeclared isopropyl alcohol is present.
LivaNova USA Inc. is recalling 150 units of Vein Irrigation Cannulas with blunt tips because internal tests identified potential breaches in the sterile barrier.
Beaming White LLC is recalling Koala Hand Sanitizer because the ethanol level is below the label claim and it contains undeclared isopropyl alcohol.
The Harvard Drug Group is recalling Metformin Hydrochloride Extended-Release Tablets due to potential NDMA impurity levels above established limits.
Beaming White LLC is recalling Koala Hand Sanitizer because the active ingredient ethanol was tested below the label claim and undeclared isopropyl alcohol was present.
Trident Seafoods is recalling Gordon Choice Imitation Crab Supreme Style because the product may contain undeclared egg white.
Kia is recalling 2020 Sedona vehicles because a loose alternator terminal nut may cause electrical arcing and increase the risk of a fire.
LivaNova USA Inc. is recalling 600 units of sterile disposable connectors because internal tests found the sterile barrier may be breached.
LivaNova USA Inc. is recalling specific lots of sterile disposable connectors because internal tests found potential breaches in the sterile barrier.
Brill Inc. is recalling 252 cases of frozen cookie dough because the product may contain undeclared walnuts, a major food allergen.
LivaNova USA Inc. is voluntarily recalling 220 units of 3/8 inch Y connectors due to a Class II defect.
LivaNova USA Inc. is recalling 240 units of sterile standalone connectors because internal tests found potential breaches in the sterile barrier.
LivaNova USA Inc. is recalling specific lots of sterile disposable connectors because internal tests found potential breaches in the sterile barrier.