State
73,718 recalls have nationwide distribution and so reach Kansas. 5,821 additional recalls listed Kansas specifically in their distribution scope.
Of the 5,821 recalls naming Kansas we have scored against our rubric, 1,053 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,485 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,821 recalls whose distribution notice names Kansas specifically. The 73,718 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Verizon is recalling 2.5 million Ellipsis Jetpack mobile hotspots because the lithium-ion battery can overheat, posing fire and burn hazards.
Meritor is recalling specific TSE T2024 Air Brake Chambers because incorrect springs may cause the pressure plate to shift, potentially leading to a loss of air pressure and increased crash risk.
Jaguar is recalling 2017-2018 and 2020 XE vehicles because missing spot welds may weaken the rear rail assembly, increasing the risk of a crash during towing.
General Motors is recalling specific Buick, Chevrolet, and GMC SUVs because side curtain air bags may not be properly attached, increasing injury risk.
General Motors is recalling specific 2014-2016 Chevrolet and GMC vehicles because a driver's seat belt cable may break, reducing safety protection.
Geo Essential LLC is recalling Wintergreen and Alleviate essential oils because the packaging is not child-resistant, posing a poisoning risk to young children.
Keystone RV Company is recalling 2020-2021 Dutchmen Aspen Trail trailers because improperly installed ramp door fasteners may strip, potentially detaching the rear door and increasing injury risk.
Wilton Industries Inc. is voluntarily recalling 1,638 units of Valentine Chip Crunch Sprinkles nationwide due to undeclared milk.
Wilton Industries is recalling Rainbow Chip Crunch Sprinkles nationwide due to undeclared milk, a major food allergen.
Wilton Industries is recalling Holiday Home Assorted Treat Toppings nationwide due to undeclared milk, a major allergen.
FDA recalls CF Delivery Dev Caps Bravo x5 capsules because they may fail to attach to the esophagus, leading to aspiration.
Smisson-Cartledge Biomedical is recalling ThermaCor 1200 Disposable Sets due to a toxicological risk assessment indicating potential aluminum ion leaching into warmed fluids.
Smisson-Cartledge Biomedical is recalling ThermaCor 1200 Disposable Sets because a toxicological assessment found potential for aluminum ions to leach into warmed fluids.
Medtronic is recalling specific Evera and Visia ICD models because a small percentage may experience a shortened Recommended Replacement Time to End of Service interval.
Smisson-Cartledge Biomedical is recalling ThermaCor 1200 Disposable Sets due to a toxicological risk assessment indicating potential aluminum ion leaching into warmed fluids.
Zydus Pharmaceuticals is recalling 1,638 packs of Acyclovir Sodium Injection due to customer complaints of crystallization in the finished product.
The FDA is recalling Bravo pH Capsule Delivery Devices because the capsule may fail to attach to the esophagus, leading to aspiration and potential hospitalization.
Goal Zero is recalling about 7,850 EC8 power cables because the connector pins can deform and overheat, posing a fire hazard. Four reports of overheating or fire have been received, with no injuries.
Nuts.com is recalling diced dried figs because they contain undeclared almonds, a major food allergen.
Wilton Industries is recalling 18,740 units of Holiday Mix Sprinkles nationwide due to undeclared milk, a major food allergen.
Wilton Industries is recalling Rainbow Chip Crunch Sprinkles nationwide due to undeclared milk, a major food allergen.
CPSC recalls 1.06 million Greenworks and Powerworks pressure washer spray guns because the plastic connector can break, causing impact injuries.
Wilton Industries is recalling 8,742 units of Autumn Assorted Treat Toppings Sprinkles nationwide due to undeclared milk.
Medtronic is recalling specific CRT-D implantable cardioverter defibrillators because a small percentage may experience a shortened time before the device reaches end of service.
CareFusion is recalling BD Alaris Infusion Pump Module Keypads and Door Assembly Kits because fluid ingress can cause unresponsive or stuck keys, potentially delaying medication infusion.