State
72,971 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 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Total Saddle Fit is recalling about 10,000 Shoulder Relief Saddle Cinches because the cinch can come apart and cause the saddle to fall off, posing a fall risk to riders. The company has received 19 reports of this defect, including one incident in which a rider fractured their ribs.
Bell Sports is recalling approximately 31,200 bicycle helmets because they fail to meet federal safety standards and may not protect wearers during a crash. Consumers should stop using the helmets immediately and contact Bell Sports for a refund.
iHerb is recalling three California Gold Nutrition iron supplement products because their bottles and blister packs do not meet federal child-resistant packaging standards, posing a risk of serious injury or death if swallowed by young children.
Peg Perego is recalling about 950 Tatamia 3-in-1 recliners, swings, and high chairs sold from November 2022 through January 2025 due to suffocation risk and safety standard violations. Consumers should stop using them immediately and contact Peg Perego for a refund.
Professional's Choice Sports Medicine Products is recalling Swivel Port equine bits from the Bob Avila collection because the bits can break during use, posing a fall hazard to riders. The company has received five reports of bits breaking but no injuries have been reported.
DR Power is recalling about 13,200 LiPRO rechargeable lithium-ion battery packs (5.0 Ah) because they can short-circuit and ignite, posing fire and burn hazards. The firm has received two reports of fire and/or overheating incidents, though no injuries have been reported.
The Coleman Company is recalling Converta camping cots and suspension stretchers because the backrest fold mechanism can pinch fingers, causing lacerations and amputations. Seven finger-pinching incidents have been reported, including two fractured fingers.
Temsa is recalling specific 2022-2025 TS30, TS35, TS45, and TS45E vehicles because an incorrectly installed lock mechanism may cause the roof hatch release handle to break, potentially delaying emergency egress.
PACCAR is recalling 2024–2026 Kenworth and Peterbilt trucks. A software fault may prevent tail brake lights, headlights, reverse lights, and turn signals from illuminating properly, and may cause lift axles to unexpectedly raise or oscillate.
Great Dane is recalling 2026 Champion dry van trailers because roll-up door operator bolts may not be tightened, increasing the risk of injury.
Chrysler is recalling certain 2023 Jeep Grand Cherokee and Grand Cherokee L vehicles because the blower motor may fail, leaving the defrosting and defogging system inoperative. This fails FMVSS 103.
Dexcom, Inc. is recalling Dexcom G7 Glucose Receiver units due to defective foam or assembly error that may cause the speaker to lose contact with the circuit board, preventing audible alerts for low or high blood glucose.
Dexcom, Inc. is recalling Dexcom One Continuous Glucose Monitoring System receivers due to potential defective foam or assembly errors that may cause the speaker to lose contact with internal components, resulting in missed audible alerts for dangerous blood glucose levels.
Dexcom, Inc. is recalling 26,291 units of the Dexcom One+ Continuous Glucose Monitoring System due to defective foam or assembly errors that may prevent audible alerts for low or high blood glucose levels, potentially leading to seizures, loss of consciousness, or death.
Dexcom G6 Glucose Receiver units may have defective foam or assembly errors that disable audible alerts for dangerously low or high blood glucose, risking seizures, loss of consciousness, or death.
General Motors is recalling certain 2024-2025 Chevrolet Blazer EV vehicles because a damaged or corroded rear parking brake harness can activate the parking brake while driving, or disable it while parked.
UMOVY ACIDO HIALURONICO dietary supplement has been recalled because it contains undeclared prescription ingredients Dexamethasone and Diclofenac. The product was marketed without FDA approval.
International is recalling certain 2019-2025 CV vehicles because the brake pressure sensor assembly may leak brake fluid into the pressure switch and short circuit. Owners are advised to park outside until repaired.
Starway International Group is expanding a recall for frozen fish products from an ineligible Vietnamese establishment. No adverse reactions have been reported.
UNAVY ACIDO HIALURONICO hyaluronic acid supplement is being recalled because it contains three undeclared pharmaceutical ingredients: Dexamethasone, Diclofenac, and Omeprazole. The product was marketed without FDA approval and poses health risks from the unlisted drugs.
BALT USA is recalling Prestige Coil System implantable embolization devices because radiopaque markers on some units were not manufactured to specification and were not visible during angiography.
Siemens is recalling 95 units of the UROSKOP Omnia X-ray system nationwide due to a resistor in the frequency inverter that may overheat and potentially ignite the plastic housing.
Ohio Medical Corporation is recalling 36 units of the GCE HEALTHCARE Zen-O lite portable oxygen concentrator due to erroneous calibration values that may cause the device's alarm for low oxygen purity to function incorrectly as the device ages.
Preat Corp is recalling Biomet 3i Certain-compatible 4.1mm Milled Titanium Abutments (Model 9001767-F) due to manufacturing defects that may cause improper screw engagement. The screw seat was positioned too high, potentially compromising the attachment of mating screws to the underlying implant.
Siemens is recalling UROSKOP Omnia Max medical devices due to a resistor in the frequency inverter that may overheat and ignite the plastic housing. Twenty-five units distributed nationwide are affected.