State
72,940 recalls have nationwide distribution and so reach Vermont. 1,983 additional recalls listed Vermont specifically in their distribution scope.
Of the 1,983 recalls naming Vermont we have scored against our rubric, 199 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 409 (21%) are Severe.
Which agencies issued them
These figures cover only the 1,983 recalls whose distribution notice names Vermont specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Lamborghini is recalling 2024-2025 Revuelto vehicles because a software error may prevent the rearview camera image from displaying, increasing crash risk.
About 21,230 Giraffe and Llama plush toys with clips sold at Hobby Lobby are being recalled because the legs can detach and release small beads.
About 148,370 Mindbodygreen Ultimate Multivitamin+ bottles are being recalled because the packaging holding iron-containing supplements is not child-resistant.
About 600 Primark The Nightmare Before Christmas Glow-in-the-Dark Coloring Sets are being recalled because the crayons have high levels of strontium and aluminum.
About 7,000 Sefudun 5% Minoxidil Hair Growth Serum Kit are being recalled because the packaging is not child-resistant as required by the Poison Prevention Packaging Act.
About 8,600 Viofairy Hair Growth Serum are being recalled because the packaging is not child-resistant as required by the Poison Prevention Packaging Act.
About 9,150 LuxJet Submersible LED Lights are being recalled because the lithium coin batteries can be accessed easily by children and the lights lack the warnings required by Reese's Law.
About 1,416 NorthStar hot water pressure washers are being recalled because the fan wheel can fail, causing abnormal burner operation that can produce smoke or bursts of flames.
About 19,890 rear wheel bolts on 2026 Trek FX+ 1 and Electra Townie Go! electric bicycles are being recalled because the bolts can break when torqued, causing wheel separation.
About 21,170 bottles of Bazic Silicone Glue are being recalled because the methanol-containing glue is not in child-resistant packaging and is incorrectly labeled "Non-Toxic".
About 320 Urban Arrow FamilyNext Pro Cargo E-Bikes are being recalled because the Fidlock buckle can fail to fully latch when used with children in the cargo area.
About 2,390 Sunneday and Blue Bay above-ground pools 48 inches and taller are being recalled because the compression strap around the pool legs may let a child climb in.
Winnebago is recalling 2026 Access travel trailers because the Gross Axle Weight Rating may be missing from the certification label, which could lead to overloading.
White Castle System is recalling 1,021 cases of White Castle Original Sliders over undeclared milk and soy.
Medline is recalling 35,694 units of the Full Electric Lightweight Homecare Bed because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.
Zero Motorcycles is recalling 2024-2025 DS, DSR, DSRP, and DSR/X motorcycles because a twisted front brake hose may leak fluid and reduce braking ability.
Ducati is recalling certain 2025-2026 Streetfighter V4 and Panigale V4 motorcycles because excessive heat may damage the rear brake hose, resulting in a sudden loss of the rear brakes.
Merit Medical Systems is recalling 864 units of its Custom Waste Management Kit Vascular Tray because the inflation device handle may detach from the syringe during a procedure.
Specialty Process Labs is recalling one lot of Thyroid, USP bulk drug substance because it is subpotent.
Merit Medical Systems is recalling its Custom Procedure Kit because the inflation device handle may detach from the syringe during a procedure.
Merit Medical Systems is recalling 4,163,123 units of the Merit Medical Inflation Device basixCOMPAK because the inflation device handle may detach from the syringe during a procedure.
Merit Medical Systems is recalling 18,897 units of its Custom Inflation Kit because the inflation device handle may detach from the syringe during a procedure.
Merit Medical Systems is recalling 328,000 units of the Allwell Angioplasty Pack because the inflation device handle may detach from the syringe during a procedure.
Graviti Pharmaceuticals is recalling 4,212 bottles of Furosemide Tablets, USP 40 mg over the presence of a foreign substance.
GE HealthCare is recalling 364 Omni Legend PET systems because an intermittent issue can produce a streaking artifact in PET clinical scan images.