State
73,503 recalls have nationwide distribution and so reach Missouri. 8,496 additional recalls listed Missouri specifically in their distribution scope.
Of the 8,496 recalls naming Missouri we have scored against our rubric, 1,344 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,198 (26%) are Severe.
Which agencies issued them
These figures cover only the 8,496 recalls whose distribution notice names Missouri specifically. The 73,503 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
CPSC recalls biOrigins sodium hydroxide products sold on Amazon from July 2020 through July 2021 due to non-child-resistant packaging and missing hazard label information. The product poses risk of chemical burns and skin/eye irritation to children.
Stokke is recalling white Clikk high chairs because the plastic seat can break, creating a fall and injury hazard to children. The company has received six reports of seat breakage, including two reports of minor bruises.
Prevost is recalling specific alternator belts because a seizing front bearing can cause the belt to overheat, increasing the risk of a fire.
Multiple brands of yogurt-covered raisins distributed nationwide are being recalled due to undeclared peanuts. Consumers with peanut allergies face a serious health risk.
Lamborghini is recalling 2020-2022 Huracan EVO and 2022 Huracan STO vehicles because insufficient transmission oil may cause clutch slippage or fire.
Audi is recalling 2021-2022 R8 vehicles because insufficient transmission oil may cause clutch slippage or fire. Owners should contact dealers for a free inspection.
Mevion S250 and S250i Proton Therapy Systems hand pendants may malfunction, causing unintended motion of the therapy couch and nozzle. This poses a risk of patient injury if they contact moving equipment.
RayStation radiation therapy planning software (versions 6-11A) may unexpectedly change jaw positions during optimization after dose or target modifications. Users should verify treatment plans carefully before delivery.
Dr. Reddy's Laboratories is recalling specific lots of Lansoprazole 15 mg delayed-release capsules nationwide because the capsules failed to dissolve properly during long-term stability testing, which could affect medication effectiveness.
Drug Depot, Inc. is recalling 24 vials of Testosterone Cypionate 200 MG/ML Injectable nationwide due to lack of sterility assurance. The product was distributed throughout the USA and Puerto Rico.
RayStation and RayPlan radiation therapy planning software may calculate incorrect radiation doses due to a source-to-skin distance calculation error. The FDA Class II recall affects 149 units distributed in the US.
Human Care USA, Inc. is recalling the Hanger-Bar 2P 45cm because the set screw may loosen due to a manufacturing defect, creating a fall hazard.
Baxter Healthcare Corporation is recalling 1,399 Liko Universal Twinbar 670 QRH patient lift accessories due to an incorrect center bolt used during assembly. The defect could cause a patient to fall during use.
Drug Depot (APS Pharmacy) is recalling testosterone cypionate/anastrozole injectable oil due to lack of sterility assurance. The recall affects 846 vials distributed nationwide.
Drug Depot recalls 1,843 vials of Gonadorelin injectable nationwide due to lack of sterility assurance. Patients should consult their healthcare provider regarding previously dispensed doses.
Drug Depot's testosterone injection product was recalled nationwide for lack of sterility assurance. Affected consumers should discontinue use and consult their healthcare provider.
Arcimoto is recalling 2019-2022 FUV, Rapid Responder, Deliverator, and Roadster motorcycles. The charging system may disable at freezing temperatures, potentially causing unexpected stalls and increasing crash risk.
Meridian Bioscience is recalling Revogene diagnostic devices due to compromised photomultiplier tubes that may produce false-positive or indeterminate test results.
Fairmont Foods is recalling Schwan's Spinach & Artichoke Dip because cartons may contain Chicken & Broccoli instead, creating potential allergen risks.
InfuTronix is recalling Nimbus PainPro ambulatory infusion pumps after an unreleased software version was installed in error. The defective units may impact patient safety.
Prevost is recalling 6,342 buses from 2010-2023 because a seizing alternator bearing can overheat and cause a fire. Owners will receive free belt replacements.
Human Care USA, Inc. is recalling the Hanger-Bar 2P 45cm due to a manufacturing defect allowing the set screw to loosen, creating a fall hazard.
Volkswagen is recalling rear hatch spoilers for 2018-2022 Tiguan long wheel base vehicles because incorrect installation instructions may cause the spoiler to detach.
Medtronic MiniMed insulin pumps may be used without programmed basal rates, causing insulin under-delivery and potentially severe high blood sugar. Patients must configure and save basal settings before use, but labeling doesn't clearly explain this requirement.
RayStation/RayPlan radiation therapy software (versions 4–11A) may incorrectly calculate radiation dose density in treatment planning. The error affects dose calculations in regions partially covered by certain structures.