State
73,509 recalls have nationwide distribution and so reach Kansas. 5,756 additional recalls listed Kansas specifically in their distribution scope.
Of the 5,756 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 5,756 recalls whose distribution notice names Kansas specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ford is recalling 2021 Mustang Mach-E all-wheel drive vehicles because a software error may cause unintended acceleration or loss of power.
Ford is recalling 2016 Super Duty trucks because dust in the steering wheel clock spring may prevent the driver's air bag from deploying.
Kuntry Kustom RV is recalling 2017-2020 Rich Specialty Trailers because propane regulators may fail, increasing pressure and fire risk.
Ford is recalling certain 2020 Escape and 2021 Corsair hybrid vehicles due to insufficient welds in the high voltage battery that may fail, causing loss of drive power and increased crash risk.
Driverge is recalling 2020-2021 Ford Transit vehicles because exposed copper in the relay module may cause a short-circuit and fire.
Blue Bird is recalling one 2023 Vision transit bus because incorrect software settings allow the engine to start while in gear, increasing crash risk.
Mitsubishi is recalling certain 2022 Outlander vehicles because the seat belt retractor may deactivate prematurely, leaving child restraints unsecured in a crash. About 2,865 vehicles are affected.
Plastic Omnium is recalling fuel tank assemblies used in Nissan and Mitsubishi vehicles because the fuel pump may fail, potentially causing an engine stall and increasing crash risk.
Ford is recalling certain 2022 Mustang vehicles with misaligned front-facing cameras that disable forward collision avoidance and other safety features. Owners should contact Ford customer service at 1-866-436-7332 to schedule free camera realignment.
Chrysler is recalling 2022 Jeep Grand Cherokee vehicles because hazard lights may flash when the brake pedal is applied, potentially confusing other drivers.
Chrysler is recalling certain 2022 Jeep Wrangler vehicles with nonfunctional side marker lights. The defect may reduce vehicle visibility to other drivers, increasing the risk of a crash.
Great Dane is recalling 2019 Freedom Platform trailers that may lack rear impact guard certification plates, potentially affecting safety compliance.
Yamaha is recalling about 4,130 Wolverine RMAX off-road side-by-side vehicles due to damaged fuel tanks that can leak fuel, creating fire and explosion risks. No injuries have been reported to date.
The Mandalorian Hand Sanitizer has been recalled nationwide due to FDA-detected benzene contamination. The recall affects 346,320 bottles with lot number 20E21.
Mickey Mouse Hand Sanitizer (ethyl alcohol 68%, 2.11 oz. bottles) is being recalled nationwide by Best Brands Consumer Products, Inc. due to methanol contamination in Lot #20D21 (expiration 06/30/2022).
Beta USA is recalling 2022 350, 390, 430, and 500 RR-S motorcycles because an incorrect front brake hose was installed, which may disconnect and cause a loss of braking.
SML Distribution is recalling 209,450 units of Skippack COVID-19 rapid test kits that were distributed without FDA authorization or clearance. The kits were distributed nationwide across Alabama, Florida, Georgia, Missouri, New York, Texas, and Wyoming.
Lupin Pharmaceuticals is recalling 1.47 million bottles of Losartan Potassium Tablets due to chemical impurities exceeding acceptable limits. The affected batches were distributed nationwide.
McKesson Corporation has recalled Lidocaine Prilocaine Cream 2.5%/2.5% because the manufacturer, Teligent Pharma, Inc., discontinued its stability study program, a deviation from manufacturing standards.
McKesson Corporation is recalling Halobetasol Propionate Ointment 0.05% nationwide after the manufacturer discontinued its stability study program, creating CGMP deviations. Over 13,200 tubes distributed in the United States, Guam, and the Northern Mariana Islands are affected.
Acera Surgical Inc is recalling 83 units of the Restrata RWM1-2X2 medical device (Lot Number 51745) due to a misprinted expiration date on the shelf-box packaging distributed nationwide.
Siemens Healthcare is recalling ADVIA Centaur Enhanced Estradiol diagnostic kits because plasma specimens may show falsely elevated results, potentially leading clinicians to misinterpret patient test results.
Macleods Pharma USA is recalling Losartan Potassium and Hydrochlorothiazide tablets due to manufacturing quality issues with chemical impurity levels above acceptable limits. Affected lots were distributed nationwide in 30-, 90-, and 1000-count bottles.
ASO LLC is recalling approximately 73,668 first aid kits sold under Equate, Meijer, and Care Science brands that contain previously recalled acetaminophen. Affected kits were distributed nationwide.
Siemens Healthcare Diagnostics is recalling Atellica IM Enhanced Estradiol diagnostic test kits (all lots) due to falsely elevated results in plasma specimens. These inaccurate results could lead clinicians to misinterpret patient data.