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.
Medtronic is recalling 10,448 Passive Biopsy Needle Kits because a manufacturing issue may cause depth stops to fail, potentially delaying surgery.
Integra LifeSciences is recalling 820 CUSA Clarity Ultrasonic Tissue Ablation Systems because the 36 kHz Sterilization Tray requires 40 minutes to dry, not the 30 minutes stated in the manual.
Volcano Corporation is recalling FFR software due to interoperability issues when connected to specific Hemodynamic Systems.
Young Dental Manufacturing Co, LLC is recalling Oral-B 5% Sodium Fluoride Varnish because the product shelf life may be shorter than indicated on the label.
Pfizer is recalling 77,100 syringes of 25% Dextrose Injection because the expiration date printed on the syringes is incorrect.
Glenmark Pharmaceuticals is recalling Clobetasol Propionate Foam because the product is not foaming or is coming out as liquid.
Glenmark Pharmaceuticals is recalling Clobetasol Propionate Foam because the product is not foaming or is coming out as liquid.
Oliver Travel Trailers is recalling 2017-2019 Elite II travel trailers because improperly tightened axle bolts may affect braking or cause wheel detachment.
Prevost is recalling 2020 X3-45 and H3-45 coach buses because driveshaft clamp bolts may not be properly tightened, which could cause loss of drive or a road hazard.
J. Crew is recalling specific boys' denim pants because small stones from the manufacturing process may remain in the pockets or waistband, posing a choking risk to young children.
Foretravel is recalling 2020 Realm and iH45 vehicles because a brake relay valve defect may increase stopping distance, raising crash risk.
Mack Trucks is recalling 2020 Anthem, Granite, and Pinnacle vehicles because steering drag link connections may be improperly installed, risking loss of steering control.
Maintainer is recalling one 2019 Custom Body Heavy Rescue vehicle because front shocks may separate, potentially causing a steering fluid leak and loss of power steering assist.
Mercedes-Benz is recalling certain 2015-2018 CLA models because the passenger air bag may not deploy properly in a crash, increasing injury risk.
Mack Trucks is recalling 2019-2020 TerraPro vehicles because improperly aimed headlamps may reduce driver visibility, increasing crash risk.
Forest River is recalling 2020 Georgetown and FR3 motorhomes because trailer hitch bolts may not be properly tightened, posing a crash risk while towing.
USDA FSIS issued a public health alert for H-E-B Butter Chicken Soup due to undeclared wheat and soy allergens.
Chrysler is recalling 2005-2006 Dodge Viper vehicles because the Occupant Restraint Control module may inadvertently deploy air bags and seat belt pretensioners, increasing injury risk.
Maintainer is recalling one 2019 Custom Body Heavy Rescue vehicle because a brake relay valve defect may cause extended stopping distances, increasing crash risk.
General Motors is recalling 2019-2020 Chevrolet Silverado 1500 and GMC Sierra 1500 trucks because excessive glue on the battery cable may cause electrical arcing, stalling, or fire.
Chrysler is recalling 2019 Ram 1500 trucks because an incorrect Tire Pressure Monitoring System sensor may prevent low tire pressure warnings from displaying.
General Motors is recalling 2019 Chevrolet Silverado 1500, GMC Sierra 1500, and Cadillac CT6 vehicles because a software error may disable Electronic Stability Control and Antilock Brake Systems without warning.
Chrysler is recalling 2018-2019 Pacifica minivans because a software error may keep the rearview camera image on the radio display after shifting out of reverse, potentially distracting the driver.
Sanofi-Aventis U.S. LLC is recalling Regular Strength Zantac 150 mg because the FDA detected the NDMA impurity in the product.
QuVa Pharma is recalling specific lots of fentanyl and ropivacaine injection bags due to the presence of glass particulate matter.