State
72,907 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 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
About 70,410 GOPO Toys pull string teething toys are being recalled after three reports of the silicone strings reaching the back of a child's throat, causing respiratory distress or choking.
Arrogantf spa drain covers sold on Amazon violate federal safety standards and pose entrapment and drowning hazards. Consumers should stop using them immediately and contact the importer for a refund.
About 1,060 Pyro Diablo "Diablo Rising" 9 Shots fireworks devices are being recalled because their pyrotechnic composition exceeds the federal limit.
SHEIN Distribution Corporation is recalling about 160 Michley children's pajamas that violate the mandatory flammability standard for children's sleepwear, posing a burn injury or death risk. No injuries have been reported.
Veseacky children's pajama sets are recalled due to burn hazards from violating mandatory safety standards for children's sleepwear. About 3,700 units were sold on Amazon from October 2020 through January 2026.
About 2,200 BABESIDE doll and stroller toy sets are being recalled because the small pacifier violates the small parts ban and the plush bear's eyes can detach.
Piaggio is recalling 2026 Liberty 50 and 150 motorcycles because a circuit fault may cause headlights to turn off, increasing crash risk.
About 5,000 Arizer Solo III Intergalactic (Black) portable vaporizers are being recalled after four reports of the internal lithium-ion battery exploding or igniting.
About 2,355 CooCooBaby Classic and Deluxe Baby Loungers are being recalled for violating the mandatory standard for infant sleep products, posing a suffocation hazard.
Farber Specialty is recalling 2025-2026 HX620 and MCXCR emergency vehicles because the touchscreen may fail, preventing the activation of exterior lights and emergency equipment.
About 3,840 Joolz Aer2 Car Seat Adapters are being recalled because they can fail to attach properly to the stroller, which may allow the car seat to fall.
Toyota Motor Engineering & Manufacturing is recalling 2026 Subaru Solterra vehicles due to a fault in the battery electronic control unit that may cause loss of drive power, increasing crash risk.
General Motors is recalling 2026–2027 Cadillac Vistiq vehicles because the third-row power seatback may fail to reverse when it encounters a person, potentially trapping them.
Doxorubicin Hydrochloride Liposome Injection, 50 mg/25 mL single-dose vials, is being recalled because of particulate matter identified as glass. 675 vials are affected.
Beekeeper's Naturals Saline Nasal Spray with propolis and xylitol, 1 fl oz, is being recalled for microbial contamination of non-sterile products. 1,680 bottles are affected.
Gas-X Extra Strength simethicone 125 mg softgels are being recalled because of contamination with a diluted propylene glycol-based coolant leaked from a machine during packaging.
TNVitamins and Doctor's Pride moringa green superfood capsules are being recalled because the product may be contaminated with Salmonella. 13,000 bottles are affected.
MIC Safety PEG Kits with ENFit Connectors, 14 Fr PULL, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall for quality issues.
Boston Scientific is removing Orca Sterile, Single Use Air/Water and Suction Valves because of a higher than anticipated occurrence of the suction button sticking. 9,750 units affected.
NexxZr T Multi A3.5 zirconia discs for all-ceramic dental restorations are being recalled because a reduced or missing dentin layer increases the risk of fracture in the mouth.
MIC Safety PEG Kits, 20 Fr PUSH OTW, catalog number 7170-20, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 901 kits affected.
CGuard Prime Carotid Stent Systems, 135 cm with a 9 mm x 30 mm stent, are being recalled because the delivery system may meet high resistance or fail to deploy the stent.
CORFLO Safety PEG Kits with ENFit Connector, catalog number 50-5320, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 72 kits affected.
CORFLO Safety PEG Kits with ENFit Connector, catalog number 50-4320, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 49 kits affected.
CGuard Prime Carotid Stent Systems, 135 cm with a 10 mm x 40 mm stent, are being recalled because the delivery system may meet high resistance or fail to deploy the stent.