State
73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Fruehauf is recalling 2018-2019 FB 53 trailers because a missing bumper gusset may allow cars to slide underneath during a crash.
Braxton Creek is recalling 2020-2021 Bushwhacker travel trailers because undersized lag bolts may allow the floor to separate from the frame, increasing crash risk.
Newmar is recalling 2018-2019 Ventana and 2021 Canyon Star motorhomes because a tire valve stem extension may damage the inner wheel, risking loss of tire pressure and a crash.
Forest River is recalling certain 2018-2021 travel trailers because the breakaway safety switch may not engage the trailer brakes during separation from the tow vehicle. This defect can cause loss of vehicle control and increased crash risk.
Forest River and Coachmen motorhomes (2018-2021) are recalled for tire valve stem damage that may cause pressure loss and crash risk. Owners should seek free replacement from the manufacturer.
Honda is recalling specific tonneau covers for 2017-2020 Ridgelines because wind may cause panels to separate, creating a road hazard.
Open Book Extracts is recalling Just Hand Sanitizer because it was labeled to contain methanol.
CareFusion is recalling Alaris System PC Unit Model 8015 infusion pumps because fluid ingress can cause unresponsive or stuck keypad keys, potentially delaying or interrupting medication infusions.
CareFusion 303, Inc. is recalling BD Alaris Syringe and PCA Modules because they may display incorrect syringe types or sizes, potentially causing infusion errors.
CareFusion 303, Inc. is recalling PC Unit Front Case with Keypad Replacement Kits because fluid ingress may cause keys to become unresponsive or stuck, potentially delaying or interrupting life-sustaining infusions.
Treehouse Foods is recalling Signature Select Chewy Granola Bars because they may contain undeclared peanut butter. The recall covers 1,202 cases distributed nationwide and to Saudi Arabia.
Maquiladora Miniara S.A. de C.V. is recalling Shine & Clean Hand Sanitizer gel because FDA testing found undeclared methanol and ethanol levels below the label claim.
Open Book Extracts is recalling Always Be Clean Hand Sanitizer because it is labeled to contain methanol. The recall covers 340,000 packs distributed nationwide.
CareFusion is recalling BD Alaris infusion pumps because fluid ingress can cause unresponsive or stuck keys, potentially delaying or interrupting infusions.
Qiagen is recalling 1,474 QIAstat-Dx Respiratory SARS-CoV-2 Panel kits due to an increased rate of false positive results for Influenza A, which may lead to inappropriate antiviral use or delayed diagnosis.
RH is recalling about 270 Industrial Three-Panel Mirrors because the panels can detach and fall, posing an injury hazard. No injuries have been reported.
Kia is recalling 2020-2021 Stinger vehicles because a fuel pump defect may block fuel flow to the engine, causing loss of power while driving and increasing crash risk.
MWE Investments is recalling Westinghouse dual fuel portable generators because they can leak fuel, posing a fire and burn hazard.
Volkswagen is recalling 23 internal use vehicles, including Golf and Passat models, because they may not meet federal safety standards. Owners will be offered a repurchase.
Monoprice is recalling Category 6 Ethernet cables that do not meet flammability standards, posing a fire hazard. Consumers should stop using the cables and contact the company for a free replacement.
Kader Exports is recalling 406,080 lbs of frozen cooked shrimp from multiple brands due to possible Salmonella contamination. The product was distributed nationwide.
Teva Pharmaceuticals is recalling Cephalexin for Oral Suspension because current Good Manufacturing Practice deviations may cause active ingredient levels to fall outside specification limits.
Teva Pharmaceuticals is recalling specific lots of Cephalexin for Oral Suspension because current Good Manufacturing Practice deviations may cause active ingredient levels to fall outside specification limits.
Ingredients Solutions Inc. is recalling 18,000 lbs of MBF-202 Carrageenan because it contains foreign fibers identified as seaweed production rope.
Talladium Inc is recalling 39 Luminesse Zirconia Discs because the linear shrinkage value on the label is incorrect and outside the acceptable range.