State
73,219 recalls have nationwide distribution and so reach Kansas. 5,755 additional recalls listed Kansas specifically in their distribution scope.
Of the 5,755 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 1,241 (22%) are Severe.
Which agencies issued them
These figures cover only the 5,755 recalls whose distribution notice names Kansas specifically. The 73,219 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
FXI recalls about 48,000 Novaform mattresses from Costco due to mold contamination from water exposure during manufacturing. The mold poses a health risk to people with compromised immune systems or mold allergies. No injuries have been reported.
Make Believe Ideas recalls seven Rainbow Road Series board books because plastic binding rings can detach, posing a choking hazard to young children. About 260,000 units were sold nationwide from March 2022 through August 2023.
Abbott Medical is recalling approximately 17,394 Proclaim DRG Implantable Pulse Generators worldwide due to reports that patients cannot exit MRI mode on affected devices. This malfunction may prevent normal device operation when mode-switching is needed.
Some Abbott Infinity 5 implantable pulse generator patients report being unable to exit MRI mode on their devices. This Class I recall affects 5,932 devices distributed globally.
Medline Industries is recalling HUDSON RCI Addipak 5mL sterile saline inhalation solution due to sterility failure. Approximately 18,000 units were distributed nationwide; the product was intended for scrap but was inadvertently shipped to customers.
General Motors is recalling certain 2023 Tahoe, Suburban, Escalade, Escalade ESV, Yukon, and Yukon XL vehicles due to improperly heat-treated rear suspension bolts that may break, risking wheel misalignment and crash.
Abbott Medical is recalling Proclaim XR 7 Implantable Pulse Generators due to a malfunction that prevents patients from exiting MRI (Magnetic Resonance Imaging) mode, potentially disrupting normal device operation and therapy delivery.
Abbott Medical recalled Proclaim Plus 7 Implantable Pulse Generators due to a defect preventing patients from exiting MRI mode. This operational failure could compromise device functionality during or after magnetic resonance imaging procedures.
Abbott Medical recalls Infinity 7 Implantable Pulse Generators due to reports that patients cannot exit MRI mode. The FDA has classified this as a Class I recall affecting devices distributed worldwide.
Abbott Medical is recalling Proclaim Plus 5 Implantable Pulse Generators (Model 3670) due to reports that patients are unable to exit MRI mode on the devices.
WEFUN Capsules 825 mg are being recalled due to contamination with sildenafil, an undisclosed active pharmaceutical ingredient not approved for the product. Distribution was nationwide.
Abbott Medical recalled the Proclaim XR 5 Implantable Pulse Generator after patients reported being unable to exit MRI mode on their devices. Approximately 113,784 units were distributed worldwide.
BE Pharmaceuticals is recalling Pantoprazole Sodium for Injection nationwide due to lack of sterility assurance caused by powder discoloration and small cracks in some vials. No illnesses have been reported.
Knorr Letras con Tomate soup mix is being recalled because it contains undeclared egg. Consumers with egg allergies should not consume this product.
ACUSON Redwood 2.0 ultrasound systems may display underestimated measurement results when using an 18L6 transducer in Dual format, potentially leading to patient misdiagnosis. 796 units are affected worldwide.
Conopco (Unilever) recalled Knorr Estrellitas con Tomate soup mix nationwide due to undeclared egg allergen. No illnesses have been reported.
BioFire Diagnostics is recalling FILMARRAY Gastrointestinal Panel software due to an increased risk of false positive Cryptosporidium test results. Approximately 61,069 devices were distributed in the US and internationally.
Medtronic Sofamor Danek USA Inc is recalling Magnifuse Bone Graft products due to incorrect size labeling on 55 pouches. Units with specific serial numbers were distributed in nine U.S. states.
Tiffin is recalling certain 2016-2024 Allegro Bus and 2017-2024 Zephyr motorhomes because the 240-volt cooktop may not be grounded, creating an electrical shock hazard. Tiffin will install a ground for the junction box at no charge.
General Motors is recalling 2014 Buick Verano and Chevrolet Cruze vehicles because side roof-rail air bag inflators may rupture, potentially causing injury from metal fragments.
Multiple frozen corn products distributed nationwide are being recalled due to potential Listeria monocytogenes contamination. Consumers should not consume the affected products.
BMW is recalling 2023 740i, 760i, and i7 vehicles because windshield wipers may fail in certain weather, reducing visibility and increasing crash risk.
Conopco is recalling Knorr Fideos con Tomate Tomato Based Pasta Soup Mix because it contains undeclared egg. The product was distributed nationwide with best-by dates through July 6, 2024.
Instrumentation Laboratory is recalling ACL TOP coagulation analyzers due to potential sample misidentification that could result in incorrect test results and alter patient management decisions.
Wabash National is recalling certain 2009-2024 dry van trailers because the rear impact guard is positioned too far forward, potentially reducing crash protection. Dealers will add an extension to the guard free of charge.