State
73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
BMW is recalling 2018-2020 X3 and 2019-2020 X4 vehicles because the instrument panel casing may not be tightened properly, posing an injury risk during air bag deployment.
Cardinal Health is recalling Monoject Hypodermic Safety Needles because they were shipped as non-sterile despite labeling indicating sterility, posing an infection risk.
Cardinal Health 200, LLC is recalling Monoject Bluntfill syringes that were shipped as non-sterile but labeled as sterile. The firm is not aware of any patient harm.
Medtronic CoreValve LLC is recalling six Simulus 750 Flexible Ring/Band Accessory Kits because demonstration units may have contacted non-human tissue.
The Boyer Corporation is recalling six brands of sodium and potassium hydroxide products because the packaging is not child-resistant, posing a risk of chemical burns.
Lupin Pharmaceuticals is recalling specific lots of oral contraceptive tablets due to failed content uniformity tests.
Verathon, Inc. is recalling 239 GlideScope Video Laryngoscope Operations & Maintenance Manuals due to a typographical error regarding disinfection instructions.
Response Biomedical Corp. is recalling RAMP Cardiac Controls because CK-MB levels decreased by up to 57% within 11 months, potentially affecting quality control results.
Braemar Manufacturing is recalling DL950 Holter Monitors because a software issue prevents new patient studies from starting.
Garza Food Ventures is recalling Siete Grain Free Burrito Size Tortillas because the sodium content is 340 mg per serving, not the 15 mg declared on the label.
Belle Chemical is recalling 100% Sodium Hydroxide Drain Cleaner because the label violates the Federal Hazardous Substance Act by omitting the word 'poison' and mandatory hazard statements.
Mayne Pharma is recalling specific bottles of Carbidopa and Levodopa Tablets because a foreign tablet was found in a bottle.
Braemar Manufacturing is recalling DL900 Holter Monitors because a software issue prevents new patient studies from starting. Existing recordings can still be downloaded.
The Binding Site Group is recalling 462 VaccZyme assay kits due to performance deterioration that may cause falsely elevated antibody results.
The Harvard Drug Group is recalling 330 cartons of Quetiapine Fumarate Extended-Release Tablets because they were packaged with the wrong package insert.
The Harvard Drug Group is recalling Quetiapine Fumarate Extended-Release Tablets because they were packaged with the wrong package insert.
The Harvard Drug Group is recalling Quetiapine Fumarate Extended-Release Tablets because they were packaged with the wrong package insert.
Integra LifeSciences is recalling 55 units of NeuraGen Nerve Guides because nonconforming product was mistakenly released for commercial use.
Lupin Pharmaceuticals is recalling specific lots of Bekyree oral contraceptives because they failed content and blend uniformity tests.
The Harvard Drug Group is recalling Quetiapine Fumarate Extended-Release Tablets because they were packaged with the wrong package insert.
American Honda is recalling about 340,000 portable generators because the inverter assembly can short-circuit in salt water, causing smoke or fire.
Yokohama is recalling specific commercial tires where the tread or bead may detach, potentially causing loss of vehicle control.
Thor Motor Coach is recalling 2020 SEQUENCE motorhomes because the transmission shifter cable may separate from the transmission, potentially causing unintended vehicle movement and increased crash risk.
Triumph is recalling 2013-2017 Trophy SE A1 motorcycles because improper brake hose routing may damage ignition wiring, causing engine stalls or lighting loss.
Volkswagen Group of America is recalling 2017-2019 Audi Q7 and 2019 Q8 vehicles because a steering shaft bolt may loosen, potentially causing a loss of steering control.