State
72,984 recalls have nationwide distribution and so reach Missouri. 8,465 additional recalls listed Missouri specifically in their distribution scope.
Of the 8,465 recalls naming Missouri we have scored against our rubric, 1,334 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,870 (22%) are Severe.
Which agencies issued them
These figures cover only the 8,465 recalls whose distribution notice names Missouri specifically. The 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
GM is recalling certain 2023-2025 Cadillac LYRIQ vehicles because front stabilizer bar bracket bolts may loosen and separate from the vehicle frame.
Honda is recalling certain 2024 Acura ZDX vehicles because passenger-side front stabilizer bar bracket bolts may loosen and separate from the vehicle frame.
Hyundai is recalling certain 2025 IONIQ 5 N vehicles because software may reduce braking performance with left-foot braking active and the vehicle may continue to accelerate.
Kramer Laboratories recalls Safetussin Max Strength Multi-Symptom Cough, Cold and Flu blister packs due to packaging that fails to resist child access. Tablets can be pushed through the foil, posing a poisoning risk to young children.
Kentfield Solid Wood Eight-Drawer Dressers can tip over if not wall-anchored, risking entrapment injuries or death to children. Modus Furniture is offering free repair kits and installation.
Fisher-Price is recalling about 15,300 Tissue Box Toys sold with 3-in-1 SnugaPuppy Activity Centers. The toy can detach and expose small brackets that pose a choking hazard to young children.
Fisher-Price is recalling about 253,000 Brunch & Go Stroller Toys because the egg component can crack and create choking hazards. No injuries have been reported; consumers should immediately stop use and request a free replacement.
Forest River is recalling 2025 Coachmen Brookstone fifth wheels because a wastewater pipe defect may allow sewer gas to enter the cabin, increasing injury risk.
Long-Haul 5L ATV fuel containers sold on Amazon.com lack required child-resistant closures, posing burn, fire, and poisoning risks to children. About 815 units sold from January 2023 through October 2024 are recalled.
About 600 magnetic puzzle crab toys sold on Walmart.com are recalled because swallowed magnets can cause serious digestive injury. Consumers should stop using them immediately and request a full refund.
E-Bully youth ATVs sold online from 2023-2024 are recalled due to defective handlebars and brakes that can cause serious injury or death.
Costway recalls about 1,400 Babyjoy Convertible 6-in-1 High Chair Activity Centers sold online at Walmart.com due to leg openings that can trap children and a tray that can disengage, posing entrapment and fall hazards.
Bebamour baby bath seats pose a drowning risk because they are unstable and may tip over or allow babies to slip out. No injuries have been reported, but consumers should stop using them immediately.
Volkswagen is recalling certain 2025 ID. Buzz vehicles because the brake system warning light may display the incorrect symbol and colour, failing FMVSS 135 and 101.
Chrysler is recalling 2025 Ram 1500 vehicles because a software error may display incorrect tire pressure messages, increasing crash risk.
MORryde is recalling specific Clip-On brackets because mounting bolts may loosen, causing steps to detach and increasing injury risk.
Forest River is recalling 2025 Coachmen Catalina travel trailers because the wastewater pipe may not extend to the exterior, allowing sewer gas to enter the cabin.
McLaren is recalling certain 2020-2025 vehicles because brake lines may be routed incorrectly, activating the brakes on the wrong side and possibly locking a rear wheel.
Draeger is recalling the Anesthesia Circuit Kit Flex EPA due to the potential for cracks to form in the breathing circuit hose. Approximately 13,620 units have been distributed domestically and internationally. Users should discontinue use of affected units immediately.
Draeger, Inc. is recalling Anesthesia Circuit Kit Flex 1 devices nationwide and internationally due to potential cracks in the breathing circuit hose that conducts anesthesia gases.
Draeger's ID Circuit Flex 220 breathing circuit for anesthesia machines may develop cracks in the hose. The recall affects 3,325 units distributed nationwide and internationally.
Draeger, Inc. is recalling 65,150 units of the VentStar Flex 220 breathing circuit due to the potential for cracks to form in the hose. A crack could affect gas delivery during anesthesia or ventilation procedures.
Draeger, Inc. is recalling the Anesthesia Circuit Kit Flex (P)2 due to the potential for cracks to form in the breathing circuit hose. This FDA Class I recall affects approximately 9,250 units distributed domestically and internationally.
Draeger's Anesthesia Circuit Kit Flex 2 is recalled because of the potential for cracks to form in the breathing circuit hose. No injuries have been reported.
Draeger, Inc. is recalling the Anesthesia Circuit Kit Flex 6 (Model MP02744) due to potential cracks forming in the breathing circuit hose. Approximately 293,660 units were distributed nationwide and internationally.