State
73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Toyota is recalling 2018-2019 4Runners because steering and suspension components may not have been properly tightened during installation, which could lead to loss of vehicle control.
Ducati is recalling 651 motorcycles because engine oil may leak into the airbox and drip onto the rear tire, increasing crash risk.
Forest River is recalling 2019-2020 Sabre trailers because a rotating pin box may contact wiring, causing electrical shorts, fire, or brake failure.
Cruiser RV is recalling 2020 South Fork recreational trailers because missing wood backers may allow the upper bunk bed to fall, posing an injury risk.
Heartland is recalling 2020 Milestone recreational trailers because missing wood backers may allow the upper bunk bed to fall, posing an injury risk.
General Motors is recalling 2019-2020 Chevrolet Equinox all-wheel drive vehicles because improperly sealed fuel tank seams may leak fuel, increasing fire risk.
General Motors is recalling replacement flip-key ignition transmitters for 2010-2015 Chevrolet Camaros because the keys may accidentally turn off the engine, causing loss of power steering and braking.
Chronicle LLC is recalling T-51b Power Armor Collectible Helmets sold by GameStop because mold may be present on the fabric liner, posing a risk of respiratory or other infections.
Exploding Kittens is recalling safety goggles sold with Extreme Edition Dodgeball game sets due to a laceration hazard from glass lenses.
Teleflex Medical is recalling specific lots of Hudson RCI Sheridan Preformed tracheal tubes because the 15 mm connector may disconnect from the tube, potentially causing insufficient oxygenation.
Plastikon Healthcare LLC is recalling specific lots of Milk of Magnesia unit dose cups because they failed bioburden testing for Total Aerobic Microbial Count.
Allergan is recalling 4 million textured breast implants worldwide after FDA safety updates linked them to a higher incidence of anaplastic large cell lymphoma.
Allergan is recalling Natrelle 133 tissue expanders due to FDA safety information regarding a higher incidence of anaplastic large cell lymphoma in patients with textured breast implants.
Allergan is recalling specific textured breast implants and tissue expanders following FDA safety updates regarding a higher incidence of anaplastic large cell lymphoma (BIA-ALCL).
Aesculap Implant Systems LLC is recalling Caiman disposable articulated instruments due to a possibility that the sterility batch was insufficiently sterilized.
Zimmer Biomet is recalling 49 units of Vanguard XP Tibial Tray 83 mm because the locking bar may not fully engage.
Zimmer Biomet is recalling 99 units of Vanguard XP Tibial Tray 79 mm because the locking bar may not fully engage.
Allergan PLC is recalling Natrelle textured breast implants and tissue expanders worldwide due to an increased risk of anaplastic large cell lymphoma.
Allergan is recalling textured Natrelle Inspira breast implants and tissue expanders following FDA safety updates linking these devices to a higher incidence of anaplastic large cell lymphoma.
Teleflex Medical is recalling specific lots of Sheridan LTS tracheal tubes because the 15 mm connector may disconnect from the tube, potentially causing insufficient oxygenation.
Allergan is recalling Natrelle tissue expanders because the FDA identified a higher incidence of anaplastic large cell lymphoma in patients with textured breast implants.
Pfizer is recalling 185,700 vials of Bacteriostatic Water for Injection due to a lack of assurance of sterility. The product was distributed nationwide in the US and Puerto Rico.
Bubbies is recalling Mochi and Cookie Dough Ice Cream Bites due to potential foreign plastic pieces. The recall covers products distributed nationwide and to Russia and Lebanon.
Allergan PLC is recalling specific textured breast implants and tissue expanders following FDA safety updates regarding a higher incidence of anaplastic large cell lymphoma (BIA-ALCL).
Allergan PLC is recalling specific textured silicone-filled breast implants and tissue expanders following FDA safety updates regarding a higher incidence of anaplastic large cell lymphoma (BIA-ALCL).