State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
General Motors is recalling 2013 Chevrolet Volt vehicles because a software update may disable cell balancing, causing a low-voltage condition that could lead to a loss of propulsion and increased crash risk.
Grand Design is recalling 2018-2019 Solitude fifth-wheel trailers because the propane line may contact a hot grill, posing a fire risk.
Chrysler is recalling 2018 Dodge Journey vehicles because the rear camera view may not appear within two seconds of selecting reverse, increasing crash risk.
Chrysler is recalling 2017-2018 Pacifica vehicles because the Manual Park Release plug can be removed without a tool, violating federal safety standards.
Chrysler is recalling 2018 RAM 1500, 2500, 3500, and Dodge Journey vehicles because the backup camera may lose image display, increasing crash risk.
Lake Michigan Distilling is recalling 190 Proof Non-Denatured Grain Alcohol due to methanol contamination that could cause serious injury or death if consumed.
Desly International Corp. is recalling Melanie Mini Cookies with Caramel Flavor because the products contain undeclared peanuts.
Desly International Corp. is recalling Melanie Liubitelskie Cookies because they contain undeclared peanuts. The recall affects 250 cases distributed across 21 states.
Draeger Medical Systems is recalling the Jaundice Meter JM-103 because users may misinterpret the out-of-range display as a zero measurement.
Hospira is recalling Naloxone Hydrochloride Injection cartridges due to the presence of particulate matter on the syringe plunger.
BLM Products is voluntarily recalling Priano Rosso Pesto Sauce due to undeclared egg and milk allergens.
Volkswagen is recalling 2003 EuroVan, Jetta, Passat, and Golf vehicles because the driver's air bag inflator may explode during deployment, posing a risk of serious injury or death.
Porsche is recalling 715 Panamera vehicles because rear anti-roll bar links may detach, potentially affecting handling and increasing crash risk.
Draeger Medical Systems is recalling 6,711 Draeger Jaundice Meter JM-105 devices because users may misinterpret the out-of-range display as a zero measurement.
Ion Beam Applications is recalling 12C units due to an issue with the AdaPTinsight software used for patient localization in radiation therapy.
Tosoh Bioscience is recalling ST-AIA PACK CK-MB assays because Asfotase Alfa (Strensiq) interferes with the test, potentially causing inaccurate results.
Tosoh Bioscience Inc is recalling ST-AIA PACK C-Peptide assays because Asfotase Alfa (Strensiq) interferes with the test, potentially causing inaccurate results.
GE Healthcare is recalling 252 units of the Centricity Universal Viewer because image series may be missing from exams without a user warning.
Tosoh Bioscience is recalling ST-AIA PACK IGE II allergy assays because Asfotase Alfa (Strensiq) can cause inaccurate test results.
Tosoh Bioscience Inc is recalling AIA-PACK TSH 3rd Generation assays because Asfotase Alfa interferes with the tests, potentially causing inaccurate results.
Tosoh Bioscience is recalling ST-AIA PACK Myoglobin assays because the drug Strensiq interferes with the test, potentially causing inaccurate results.
Santajoy Ornament & Giftware Co. is recalling E-Z Illuminations laser projectors because they may emit radiation exceeding federal standards for Class IIIa products.
Tosoh Bioscience Inc is recalling ST-AIA PACK IRI assays because Asfotase Alfa (Strensiq) interferes with the tests, potentially causing inaccurate results.
Mako Surgical Corporation is recalling 575 units of the Restoris MCK Onlay Insert Extractor because the hinge pin may disassociate.
Tosoh Bioscience Inc is recalling ST-AIA PACK CEA assays because Asfotase Alfa (Strensiq) interferes with the test, potentially causing inaccurate results.