State
73,824 recalls have nationwide distribution and so reach Kansas. 5,822 additional recalls listed Kansas specifically in their distribution scope.
Of the 5,822 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 1,486 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,822 recalls whose distribution notice names Kansas specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Lippert Components is recalling specific 7000lb and 8000lb Brake Axles because loose flange nuts may cause brakes to lock up or fail to engage, increasing crash risk.
Wells Enterprises is recalling specific lots of Blue Bunny Hoppin' Holidoodle ice cream due to potential Listeria monocytogenes contamination.
Café Valley Inc. is voluntarily recalling 1,170 cases of Banana Nut mini muffins mislabeled as Lemon Poppy Seed because they may contain undeclared walnuts.
Hospira is recalling specific lots of Fentanyl Citrate Injection ampules because broken tips may compromise sterility.
AtriCure is recalling COBRA Fusion Ablation Systems because a part may separate and remain in the body, potentially causing permanent impairment or damage.
Seth Ellis Chocolatier is recalling Free2b Sun Cups Chocolate due to potential contamination with milk ingredients. The recall covers 189 master cases distributed nationwide.
BioLite is recalling BaseLanterns and BaseLantern XLs because the lithium-ion batteries can overheat and catch fire. One report of minor property damage has been received.
VistaPharm is recalling Lactulose Solution, USP, 10 g/15 mL, because bulk solution tested positive for Burkholderia cepacia bacteria.
Pfizer is voluntarily recalling 2,666 bottles of LEVOXYL (levothyroxine sodium) 200 mcg tablets nationwide because the product is superpotent.
Merit Medical Systems is voluntarily recalling 178 Fluid Management Sets due to a compromised sterile barrier.
Merit Medical Systems is recalling 53 Procedure Kits due to a compromised sterile barrier. The kits were distributed nationwide to specific states and Japan.
CSC Motorcycles is recalling 2015-2016 Cyclone motorcycles because they may lack a required label reminding users to use DOT 4 brake fluid.
Hologic is recalling SURESOUND22 uterine sound multipacks because a breach in the sterile barrier compromises product sterility.
EN-R-G Foods is recalling Cherry Lime, Raspberry, and Juneberry Protein Chews due to consumer complaints of nausea and vomiting after consumption.
Merit Medical Systems is recalling 40 Manifold Kits (Catalog No. K09-11867AP) because the sterile barrier is compromised, posing a risk of infection.
Merit Medical Systems is voluntarily recalling 130 MeriTrans Pressure Monitoring Kits because a compromised sterile barrier may affect product sterility.
IMUSA is recalling about 17,500 espresso makers because the filler cap can crack or pop off, posing burn and impact risks.
Toshiba American Medical Systems is recalling Aquilion Prime CT systems because cooling oil in the x-ray tube heat exchanger may leak during operation.
Cummins is recalling 164 model year 2015-2016 generator sets because door hinges may fail, causing doors to detach and create road hazards.
Philips is recalling 1,363 CT scanners because the patient support tabletop may fail to move horizontally during scans due to a mechanical linkage failure.
LGS Industries is recalling 2017 Pace, Cargo Express, and Look cargo trailers because a defective weld could cause the ramp door bracket to detach, creating a crushing hazard.
EN-R-G Foods is recalling Cherry Lime Protein Chews due to consumer complaints of nausea and vomiting after consumption.
Merit Medical Systems is voluntarily recalling specific Procedure Kits due to a compromised sterile barrier, which may affect the sterility of the contents.
Siemens is recalling Dimension Vista Chemistry 1 Calibrators (lots 5GM081 and 5GM082) because they may cause discrepant low calcium recovery in quality control and patient samples.
Bausch + Lomb is recalling PeroxiClear Peroxide Solution because the product was found to contain excess residual levels of hydrogen peroxide.