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.
Morrison Milling is recalling FBR Batter Mix because it may contain small metal fragments from a wire mesh sifter.
Morrison Milling is recalling HEB Rosemary Olive Oil with Sea Salt Cornbread Mix because it may contain small metal fragments from a wire mesh sifter.
Morrison Milling is recalling Morrison's Country Style Buttermilk Pancake Mix because it may contain small metal fragments from a wire mesh sifter.
Morrison's Texas Style Honey Sweet Cornbread Mix is being recalled because it may contain small metal fragments from a wire mesh sifter.
Impax Laboratories is recalling 42,239 bottles of Fenofibrate Capsules (Micronized) 200 mg because some bottles have incorrect or missing lot and expiration dates.
Polaris is recalling about 133,000 RZR recreational off-highway vehicles because they can catch fire while driving, posing fire and burn hazards.
Brunton Outdoor Inc. is recalling Impel and Impel 2 rechargeable battery packs because they can overheat and catch fire during charging.
Forest River is recalling 2016 Glaval Entourage and Universal buses because seats may separate from the base frame due to bolt failure, increasing injury risk in a crash.
Forest River is recalling 2016 Elkhart ECE4 transit buses because seats may separate from the base frame due to bolt failure, increasing injury risk in a crash.
New Flyer is recalling specific transit buses because a software defect may cause the rear door to open unexpectedly while the bus is moving, increasing injury risk.
Flying Tiger Copenhagen is recalling wooden blocks and giraffe toys because parts can detach and pose a choking hazard to young children.
Riverside RV is recalling 2015 White Water Retro travel trailers because a narrow axle may cause tire failure, increasing crash risk.
Miniland Educational is recalling Moogy plush toys because buttons can detach, posing a choking hazard to young children.
Nissan is recalling 2014-2016 Rogue vehicles because rear lift gate support stays may corrode and break, increasing injury risk.
Toyota is recalling 58,515 model year 2016 Camry and Avalon vehicles because the occupant classification system may be improperly calibrated, potentially preventing front passenger air bags from deploying.
Forest River is recalling 2015-2016 Shasta Airflyte RVs because the dinette table may lack adequate support and fall, potentially causing injury.
Steve Johnson Induction Solutions is recalling specific nitrous oxide solenoid valves because end stops may break under pressure, posing an injury risk.
Forest River is recalling 2008-2016 Glaval Bus transit models because rear emergency exit labels are not placed within 16 centimeters of release mechanisms, potentially hindering quick escape.
Staples is recalling about 2,000 Back in Motion office chairs because they can tip over when leaning back, posing a fall hazard.
Academy Sports + Outdoors is recalling Outdoor Gourmet marinade injectors because small metal shavings may be present inside the product.
Fisher-Price is recalling about 34,000 infant cradle swings because the seat peg may not be fully engaged, allowing the seat to fall unexpectedly.
Vascular Solutions is recalling Guardian II Hemostasis Valves because the low-pressure seal may fail, potentially allowing air into the device and causing an air embolism.
Sweetwater Farms LLC is recalling sprouted mung beans due to potential Salmonella contamination. The product was distributed in Arkansas, Kansas, and Oklahoma.
Meditech Laboratories is recalling Formula 4 Injection vials due to incomplete data regarding production sterility.
Meditech Laboratories is recalling Formula 2 vials because an active ingredient expired before the labeled Beyond Use Date.