State
73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Honda is recalling approximately 56,000 Pioneer 1000 recreational off-highway vehicles because an incorrectly installed throttle body can ignite, posing fire and burn hazards.
H.I.S. is recalling Self-Esteem brand girl's clothing sets because the included pendant necklaces contain lead levels exceeding federal bans. No injuries have been reported.
Mountain Warehouse is recalling about 1,000 children's water bottles because the spout can detach, creating a choking hazard. No injuries have been reported.
Chrysler is recalling 2018 Jeep Wrangler four-door vehicles because the right rear door latch may be misaligned, potentially preventing the door from latching properly.
A. O. Smith is recalling specific 30-gallon gas water heaters sold at Lowe's in California because the flame arrestor may fail, posing a fire risk.
Lifetone Technology is recalling HLAC151 Bedside Fire Alarm and Clocks because the optional bed shaker may fail to operate during a fire emergency.
Silverstone is recalling Ride Eazy DOT Sleek helmets because they may not adequately protect wearers in a crash, increasing injury risk.
Pharm D Solutions is recalling Caffeine and Sodium Benzoate Injection 125 mg/125 mg/mL due to a lack of assurance of sterility. The recall covers 567 milliliters distributed nationwide.
Pharm D Solutions is recalling Bi-Mix Injection due to a lack of assurance of sterility. The product was distributed nationwide.
Dexter Axle Company is recalling specific trailer axles because inner hub bearings may lack sufficient grease, risking overheating and failure.
Pharm D Solutions is recalling Trimix BM3 Papaverine 30 mg/Phentolamine 1 mg Injectable because the agency could not ensure the product was sterile.
Pharm D Solutions is recalling 29 bottles of Calcium Gluconate 1% Eyewash because the company cannot ensure the product is sterile.
Pharm D Solutions is recalling 179 vials of Sermorelin/Ipamorelin powder because the company cannot ensure the product is sterile.
Pharm D Solutions is recalling 420 vials of Sermorelin/GHRP-2/GHRP-6 powder nationwide due to a lack of assurance of sterility.
Pharm D Solutions is recalling specific lots of Trimix T-106 aqueous solution because the company cannot ensure the product is sterile.
Avella of Deer Valley is recalling 1,360 bags of Morphine in NS due to a lack of assurance of sterility. The product was distributed nationwide.
Siemens is recalling 35 Multix Fusion radiographic systems because steel cables in the lifting column may rupture without triggering the safety lock, causing the arm to drop unexpectedly.
Pharm D Solutions is recalling 881 vials of HCG Lyopholized 1200 IU Injectable nationwide due to a lack of assurance of sterility.
Siemens is recalling 142 Ysio radiographic systems because steel cables may rupture, causing the tube arm to drop unexpectedly during patient positioning.
Pharm D Solutions is recalling Ascorbic Acid 500 mg/mL Solution due to a lack of assurance of sterility. The recall affects nationwide distribution.
Pharm D Solutions is recalling 765 vials of HCG 3000 Unit Powder nationwide due to a lack of assurance of sterility.
Leica Microsystems is recalling BOND Slide Labeler Zebra Printers because the power supply unit may overheat or cause a fire due to an improperly-mixed phosphorus compound.
Pharm D Solutions is recalling Prostaglandin E1 150 mcg/mL Injectable because the agency could not ensure the product was sterile.
Pharm D Solutions is recalling 108 vials of Sermorelin/GHRP-2/Theanine/Mannitol powder because the company cannot ensure the product is sterile.
Pharm D Solutions is recalling specific lots of a compounded medication solution because the company cannot guarantee the product is sterile.