State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
NutraKey, Inc. is recalling VPro Raw Plant Protein, Chocolate, because it contains undeclared soy. The recall covers 17,730 units distributed nationwide.
Whole Foods Market is recalling Maytag Blue Cheese products due to possible contamination with Listeria monocytogenes.
Actavis is recalling specific lots of amphetamine tablets because they failed impurity specifications. Consumers should stop using the product and contact their pharmacist.
Focus Diagnostics is recalling Simplexa HSV 1&2 Direct Amplification Discs because they may cause false negative or positive results and error codes.
NutraKey, Inc. is voluntarily recalling VPro Raw Plant Protein, Vanilla, due to undeclared soy. The product was distributed nationwide.
Focus Diagnostics is recalling Simplexa Group A Strep Direct Amplification Discs because they may cause false test results or error codes.
Synthes (USA) Products LLC is recalling specific lots of Titanium Low Profile Neuro Screws because the thread height is undersized, potentially compromising the device's structural integrity.
Sweetwater Farms LLC is recalling specific lots of 100% Pure Sprouted Clover due to potential Salmonella contamination. The product was distributed in Arkansas, Kansas, and Oklahoma.
Mercedes-Benz is recalling 2016 SLK300 vehicles because a backup power supply for the ignition switch may not be properly connected, creating a risk of the vehicle rolling.
Karavan is recalling 2016 KPSD trailers because a defective axle spindle flange may bend, causing excessive tire wear and increasing the risk of tire failure and a crash.
NutraKey, Inc. is voluntarily recalling VPro Raw Plant Protein nationwide due to undeclared soy, a major food allergen.
Actavis Elizabeth LLC is recalling 257,746 bottles of Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 20 mg, because they failed impurity specifications.
MicroAire Surgical Instruments is recalling 37 units of the PAL-R4011XL French Rasp aspiration cannula because they bent or broke during surgery.
ScottCare is recalling 9,067 TeleSentry batteries after a complaint that one exploded while recharging. The batteries are used in cardiac monitoring devices.
Meditech Laboratories is recalling Formula 9 Injection vials due to incomplete production data regarding sterility assurance.
NutraKey, Inc. is recalling VPro Raw Plant Protein, Mocaccino, because it contains undeclared soy. The product was distributed nationwide.
Meditech Laboratories is recalling Formula 0 Injection due to incomplete production data regarding sterility assurance.
Meditech Laboratories is recalling Formula 2 Injection vials because one ingredient exceeded assay specifications, making the drug superpotent.
Sweetwater Farms LLC is recalling sprouted alfalfa due to potential Salmonella contamination. The product was distributed in Arkansas, Kansas, and Oklahoma.
Hillsboro is recalling 2016 aluminum utility trailers because improperly installed axle hardware may cause the axle to shift, increasing crash risk.
Therakos Inc is recalling 729 units of the CELLEX Photopheresis System, Lot D342, due to an increased trend in tubing leaks within the pump tubing organizer.
Yamaha is recalling about 7,000 model year 2016 YXZ1000R utility vehicles because water in the throttle cable can freeze, preventing the throttle from returning to idle and causing loss of control.
AngioDynamics is recalling 136 NAMIC Convenience Kits because the needle inner lumen is too small to accept the intended 0.038-inch guidewire.
Fresenius Medical Care is recalling 1,650 Hemoflow F3 Dialyzers due to a potential header leak caused by improper torque.
Philips is recalling eValueMed infant heel warmers and transport mattresses because they lack expiration dates and warnings about overheating risks.