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.
AuroMedics Pharma LLC is recalling Mirtazapine 15 mg tablets that were incorrectly labeled as 7.5 mg. The error affects 500-count bottles distributed nationwide.
Harrison Gypsum, LLC is recalling Terra Alba Calcium Sulfate Dihydrate in various bag and bulk sizes due to possible contamination with Salmonella.
Cain Food Industries is recalling ASCORBO 150 Powder due to possible Salmonella contamination. The product was distributed in seven states.
Cain Food Industries is recalling 1,000 pounds of OXIBAKE YF due to possible Salmonella contamination. The product was distributed in seven states.
Jubilant Cadista Pharmaceuticals is recalling 1,824 bottles of Amantadine Hydrochloride Tablets because a foreign object was found in a single tablet.
Cooper Tire is recalling specific Evolution Tour, Mastercraft, Hercules, Starfire, and Stratus tires due to an improper sidewall component that may cause tire deflation and tread separation.
Cain Food Industries is recalling 2,000 pounds of SLB-R Powder due to possible Salmonella contamination. The product was distributed in seven states.
Cain Food Industries is recalling 2,200 pounds of BETA P-130 due to possible Salmonella contamination. The product was distributed in seven states.
Anazao Health is recalling Fentanyl Citrate products because environmental sampling detected Talaromyces rotundus, a fungus, indicating a lack of processing controls.
Maintainer is recalling 2015-2019 Custom Body Heavy Rescue vehicles because unprotected air pressure control lines may cause unexpected brake application.
Integra LifeSciences is recalling 820 C7000 CUSA Clarity Ultrasonic Tissue Ablation Systems because the 36 kHz Sterilization Tray does not meet the 30-minute drying criteria stated in the manual.
Paragon 28, Inc. is recalling 64 Titan 3-D Wedge implant kits because they are permanently mislabeled with the wrong size, which could cause surgical delays.
Integra LifeSciences is recalling 820 CUSA Clarity Ultrasonic Tissue Ablation Systems because the 36 kHz Sterilization Tray does not meet the required drying time criteria.
Boston Scientific is recalling 179 Habib EUS RFA electrode tips because capacitive coupling may cause unintended thermal injury to tissue outside the treatment area.
Abbott Medical is recalling 8,940 radiofrequency grounding pads nationwide because an incorrectly oriented release liner may leave film on the pad, interfering with skin contact and causing uneven heating.
Kraft Heinz is recalling Breakstones Lowfat Large Curd Cottage Cheese due to the potential presence of red plastic and metal pieces introduced during production.
Ethicon Endo-Surgery Inc is recalling Ligamax 5 mm Endoscopic Multiple Clip Appliers due to potential holes in the Tyvek lidding that could breach sterility.
Forest River is recalling 2018-2020 Dynamax Isata motorhomes because slide-out mechanisms may activate unexpectedly, increasing the risk of injury or a crash.
Werner Gourmet Meat Snacks is recalling Jolly Rancher hard candies due to undeclared soy lecithin. The product was distributed nationwide and in Canada.
Kraft Heinz is recalling Breakstones 4% Milkfat Large Curd Cottage Cheese due to the potential presence of red plastic and metal pieces introduced during production.
Cruise Car is recalling 2019 Moke vehicles because they may have windshields with incorrect glass quality ratings, which could affect driver visibility and increase crash risk.
Ford is recalling 2020 F-150 trucks because the 17-inch spare tire may be damaged, increasing crash risk. Dealers will replace the tire free of charge.
Getinge is recalling 3,633 units of Quadrox-iD Pediatric Diffusion Membrane Oxygenators because the sterile barrier system may be compromised.
Ford is recalling 2006-2010 Fusion, Milan, MKZ, and Zephyr vehicles because ABS valves may fail to close, increasing stopping distance and crash risk.
Conformis, Inc. is recalling the iTotal CR Knee Replacement System because the polyethylene inserts did not securely fit into the cobalt chrome tray implant.