State
73,376 recalls have nationwide distribution and so reach Kansas. 5,755 additional recalls listed Kansas specifically in their distribution scope.
Of the 5,755 recalls naming Kansas we have scored against our rubric, 1,056 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,477 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,755 recalls whose distribution notice names Kansas specifically. The 73,376 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
TruVision Health is recalling TruWeight and Energy Gen 2+ because it contains DMHA and hordenine, which FDA has determined are not acceptable dietary ingredients. No illnesses have been reported.
TruVision Health LLC is recalling truControl W/Dynamine because the product contains DMHA and/or hordenine, which FDA has determined are not acceptable dietary ingredients.
Siemens Luminos Agile Max fluoroscopic imaging systems may occasionally display incorrect radiation dose information under certain unlikely circumstances. The manufacturer states there is no impact on clinical workflow or diagnosis. The error only occurs in systems with a second overhead X-ray tube.
Siemens Healthcare Diagnostics is reassigning Atellica CH Toxicology Calibrators due to a positive bias. The affected calibrators were distributed in the US and internationally across multiple countries.
Teva Pharmaceuticals is recalling Fentanyl Buccal Tablets (200mcg) due to missing or incorrect package inserts. Patients should contact their healthcare provider if they have affected product.
Siemens Luminos dRF Max fluoroscopic imaging systems may occasionally display incorrect radiation dose measurements during certain operating conditions. The manufacturer states the error does not affect diagnosis or workflow.
LUMINOS Lotus Max fluoroscopic systems may sporadically display incorrect radiation dose measurements. The error only occurs with secondary X-ray tubes and does not affect diagnosis or workflow.
Amerisource Health Services LLC recalls 63,335 bottles of Glimepiride Tablets nationwide due to manufacturing practice deviations identified during FDA inspection.
Teva Pharmaceuticals USA Inc is recalling Fentanyl Buccal Tablets 800mcg due to incorrect or missing package inserts. The recall affects 3,032 units distributed nationwide.
Teva Pharmaceuticals is recalling Fentanyl Buccal Tablets 100mcg due to incorrect or missing package inserts in affected cartons. Patients should verify proper labeling or contact their pharmacy.
Teva Pharmaceuticals is recalling Fentanyl Buccal Tablets 600mcg due to incorrect or missing package inserts in 1,908 units distributed nationwide across multiple lot numbers.
Amneal Pharmaceuticals recalls Methylprednisolone Acetate Injectable Suspension due to incorrect NDC number on product cartons. The typographical error appears on secondary packaging only; the medication vial itself is unaffected.
Wabash National is recalling 2024 DVDBHPC and DVCVHPC dry van trailers because improperly welded king pins may detach, increasing crash risk.
NHTSA is recalling 2017-2020 Alfa Romeo Giulia and 2018-2020 Stelvio vehicles with carbon ceramic brakes due to a risk of rotor fracture and decreased brake performance.
Toyota is recalling 2022-2023 Corolla Cross vehicles because the instrument panel may lack required perforations, preventing proper front-passenger airbag deployment in a crash.
Tesla is recalling 2022-2023 Model Y vehicles because a loose steering wheel fastener may allow the wheel to disconnect, increasing crash risk.
Ford is recalling 2015-2019 Lincoln MKC vehicles because a battery monitor sensor may short-circuit and overheat, causing a fire in the engine compartment.
Forest River is recalling 2023 East to West Della Terra and Silver Lake travel trailers because an incorrectly installed furnace may cause a gas leak inside the cabin.
Knapheide is recalling 2022-2023 trucks equipped with certain Warn winches because water intrusion can cause the winch to operate unintentionally, increasing injury risk.
Ford is recalling certain 2020-2023 Escape, 2022-2023 Maverick, and 2021-2023 Corsair vehicles due to a 2.5L engine defect that could cause an engine compartment fire. No injuries have been reported.
Ford is recalling certain 2019-2023 Ranger, 2022-2023 Bronco, and 2023 F-250 SD vehicles with TREAD labels stating incorrect load carrying capacity, which could result in vehicle overload and increase crash risk.
Ducati is recalling 2020-2023 Panigale V2 motorcycles because the dashboard may automatically switch headlights to daylight running lamps, reducing night visibility.
Certain 2021-2023 Keystone Arcadia travel trailers lack a backer board behind the wardrobe cabinet, potentially allowing the slide room to extend and cause injury. Dealers will install steel brackets to secure the slide room at no cost.
Autocar is recalling 2021-2023 Xpeditor commercial trucks due to incorrectly assembled right-side door latches that may open unexpectedly during operation. Owners should contact Autocar for a free inspection and reassembly.
Jaguar is recalling certain 2019-2024 I-PACE vehicles because the high-voltage battery may overheat, increasing the risk of fire. Owners should park and charge vehicles outside until repairs are complete.