State
72,936 recalls have nationwide distribution and so reach Kansas. 5,723 additional recalls listed Kansas specifically in their distribution scope.
Of the 5,723 recalls naming Kansas we have scored against our rubric, 1,045 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,228 (21%) are Severe.
Which agencies issued them
These figures cover only the 5,723 recalls whose distribution notice names Kansas specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Philips is recalling the Allura Xper FD10C because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Medtronic is recalling Paradigm insulin pumps models MMT-712 and MMT-715 because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
SIGNA Premier MRI systems are being recalled because they may have been built or serviced with ferrous steel fittings instead of non-ferrous brass on the magnet rear.
Intuitive Surgical is recalling da Vinci S and Si Mega Needle Driver Instruments following increased complaints of broken or frayed grip cables in reusable instruments.
Medtronic is recalling MiniMed 670G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Medline is recalling four bronchoscopy and laryngoscopy kits because they contain recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.
The Finesse BTK Multicath injectable angioplasty balloon catheter is being recalled because of the potential for the balloon not to meet burst specifications.
Burlington Medical is recalling protective vests because of the potential for attenuation degradation over time, decreasing the lifespan of the garment.
Philips is recalling Vue Motion V12 because mis-ordered frames during dynamic cine runs may cause image frames to display out of sequence.
Burlington Medical is recalling BAT (Breast, Axilla and Thyroid) Coverage because of the potential for attenuation degradation over time.
Mentor is recalling Artoura Breast Tissue Expanders in the smooth ultra high profile range because the infusion sets may contain a dull or blunt needle tip.
Medline is recalling the Anterior Hip Pack because it contains recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.
Philips is recalling the Allura Xper FD20 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Burlington Medical is recalling half aprons because of the potential for attenuation degradation over time, decreasing the lifespan of the product.
Philips is recalling the Allura Xper FD20 Biplane because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Forest River is recalling 2026 Westbrook and Avenger travel trailers because the Federal Placard label may list an incorrect dry weight, potentially leading to vehicle overloading.
BD is recalling the Kiestra ReadA because after a system reboot one or more modules may become unreachable via the remote connectivity interface, delaying plate retrieval.
Bombardier Recreational Products is recalling 2025 Can-Am Origin electric motorcycles because a front brake caliper support may fail, causing inoperative front brakes.
Pierce Manufacturing is recalling 2015-2026 aerial firetrucks because a faulty light may falsely indicate the vehicle is stable, increasing injury risk during operation.
Hyundai is recalling certain 2023–2026 Genesis G90 vehicles because driver and passenger seat belt anchors may detach. Detached anchors cannot adequately restrain occupants in a crash, increasing injury risk.
Greenpower is recalling 2020-2024 Nano Beast and 2021-2024 Beast school buses because a warning label on the cross-view mirror may be missing, potentially increasing crash risk.
USDA FSIS retracted a public health alert for Dorada chicken nuggets after follow-up testing confirmed the initial lead result was a laboratory error.
Mercedes-Benz is recalling specific 2018-2020 E-Class and S-Class models because the drive shaft universal joint may break, causing a sudden loss of drive power and increasing crash risk.
Autocar is recalling 2025-2026 Xpeditor vehicles because the winter front cover may interfere with the forward collision warning system, increasing crash risk.
Sleepy Customs LLC is recalling IS300 Slave Cylinder Conversion Kits because the adapter plate may separate, causing loss of clutch function and increasing crash risk.