State
73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
The 2021 Ford E-350 may have inadequate rear axle differential fluid, risking driveshaft separation and loss of drive. Ford will inspect and adjust or replace the rear axle assembly at no cost.
Ford is recalling 2015-2016 F-150 trucks with 3.5L GTDI engines because a misplaced block heater could damage a cable, increasing the risk of a fire.
Ford is recalling 2018-2020 F-150 trucks because daytime running lamps may fail to dim, reducing visibility for other drivers and increasing crash risk.
CHTC Bus Group is recalling 2016-2018 HT-35 and HT-45 buses because their wheelchair platform lifts failed to complete the required compliance certification process.
Meritor is recalling specific steer axles due to insufficient lubrication that may damage wheel end bearings. This defect could cause the wheel to separate, leading to a loss of vehicle control.
SMC Trailers is recalling 2019-2020 Laramie trailers because the Federal Placard lists the incorrect tire PSI, which may lead to overinflation and tire failure.
Browning is recalling approximately 1,265 leather pistol holsters because the design can inadvertently change the firearm's safety switch position, posing an injury risk.
Interamerican Auto Parts is recalling specific KelvinHID HID bulbs because their light output may be incorrect and blind oncoming traffic, failing federal safety standards.
Kolcraft is recalling inclined sleeper accessories for two bassinet models to prevent infant suffocation. Consumers should stop using the accessory immediately.
Teleflex Medical is recalling 127,293 Hudson RCI Comfort Flo Humidification Systems nationwide due to a potential risk of water flooding the column and entering the circuit during high-flow oxygen therapy.
Teleflex Medical is recalling 95,696 Hudson RCI Comfort Flo Humidification Systems due to a potential risk of water flooding the column and entering the patient circuit during high-flow oxygen therapy.
Pacific Medical Group is recalling 466 Toco M2734A fetal monitors serviced with unverified non-OEM components that may fail to detect fetal distress or cause burns.
Terumo is recalling 33 Advanced Perfusion System 1 Roller Pumps because the pump shafts may fail, potentially causing the pump to stop during surgery.
Medtronic is recalling specific 640G insulin pumps due to a loose reservoir that may cause incorrect insulin delivery.
Taro Pharmaceuticals is recalling Lamotrigine Tablets 100 mg because they were cross-contaminated with enalapril maleate. The affected lot was distributed nationwide in the U.S. and Puerto Rico.
Terumo is recalling 11 Advanced Perfusion Assembly Pump Guts units because pump shafts may fail, potentially causing the pump to stop during surgery.
Medtronic is recalling MiniMed 630G Systems with SmartGuard because a broken or missing retainer ring can cause the insulin reservoir to become loose, leading to incorrect insulin delivery.
Teleflex Medical is recalling Rusch Greenlite Single-Use Metal Laryngoscope Blades because they may break at a welded joint during setup or use.
Pacific Medical Group is recalling Loop-Style Tocotransducers serviced with unverified non-OEM components, which may cause inaccurate fetal monitoring or patient burns.
AuroMedics Pharma LLC is recalling 30,432 bottles of Amoxicillin and Clavulanate Potassium tablets because a customer complaint identified a nylon cable tie as a foreign substance.
Pacific Medical Group is recalling 6,481 Button-Style Ultrasound Transducers serviced with unverified non-OEM components. The defect may cause inaccurate fetal and maternal monitoring or patient burns.
Pacific Medical Group is recalling 5,897 ultrasound transducers serviced with unverified non-OEM components, which may cause inaccurate monitoring or patient burns.
Akorn Inc is recalling 16,078 bottles of Hydrocortisone and Acetic Acid Otic Solution due to low assay results for the hydrocortisone component.
Tytek Medical Inc is recalling 3,565 PneumoDart devices because a defect involving an occluded needle was discovered during a training exercise.
Efficient Laboratories is recalling 5,249 bottles of Rompe Pecho CF Cold & Flu with Honey due to microbial contamination. The product was distributed nationwide in the USA.