State
72,907 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 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Topyond pool drain ports with covers violate federal entrapment protection standards and pose serious injury or death risks from entrapment and drowning. Consumers should stop using pools with these drain ports immediately.
Target has recalled approximately 49,000 Gigglescape Under the Sea Popping Toys because the clear plastic dome can detach, exposing small plastic balls that pose a choking hazard. One child began to choke after the dome detached.
Altec is recalling 2022-2026 Service Body vehicles because inverter AC wiring may be damaged, creating a short circuit and fire risk.
Winco Fireworks International recalls Unity 7 Shot 200 Gram Aerial Cake firework devices that can tip over, creating risk of serious injury from explosion and burns. About 87,120 units sold at Pyro City and independent fireworks stores nationwide from January through May 2026 are affected.
Winco Fireworks International is recalling Roman Candles 8 Shot 3-Pack firework devices because the fireworks can malfunction and shots can blow out the side of the tube, posing a risk of serious injury from explosion and burn hazards. No injuries have been reported.
AMASKY Nursing Pillows, sold on Amazon from January to March 2026, violate safety standards and can obstruct infant breathing, posing a serious risk of suffocation. No injuries have been reported.
CPSC has recalled POPOOO Jungle Safari LED Finger Lights sold on Amazon because the toys contain easily accessible button cell batteries that can cause serious injury or death if swallowed. No injuries have been reported.
Warn Industries is recalling Wireless Remote Kits (part numbers 90287 and 90289) because the remote control may be incompatible with legacy winches, causing unexpected movement and increasing injury risk.
Medline Industries recalled multiple convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA clearance. The company identified these modifications and notified the FDA of the deviation from the approved 510(k) design.
George J Howe Company, Inc. is recalling 25-pound cases of sunflower seeds due to the presence of undeclared cashew, a tree nut allergen. The product was distributed across multiple states.
CareFusion 213, LLC is recalling ChloraPrep One-Step (chlorhexidine gluconate and isopropyl alcohol) topical applicators due to non-sterility caused by the presence of Aspergillus penicillioides fungal contamination.
Medline Industries is recalling two models of Convenience Kits (ACC011142 and DYNJ8407) distributed nationwide. The kits contain injectable anesthetics that were recalled due to quality issues found during an FDA inspection of the supplier.
Spring & Mulberry Inc. is recalling Spring & Mulberry Mango Chili Date-Sweetened Chocolate bars nationwide due to potential Salmonella contamination. Consumers should not consume the product and should dispose of it or return it.
Abiomed is recalling Impella CP Set with SmartAssist (10th Generation) containing 14Fr Low Profile Introducer Kits due to potential thrombus (blood clot) formation during prolonged use of the introducer.
Honda is recalling 2026 Pilot and Passport vehicles because improperly tightened rear subframe bolts may lead to vehicle instability or detachment, increasing crash risk.
Abiomed is recalling 3 units of the 14 Fr x 13 cm Low Profile Introducer Kit for Impella CP due to potential for blood clot formation during prolonged use.
Spring & Mulberry Inc. is recalling Sea Salt Date-Sweetened Chocolate bars due to potential Salmonella contamination. Approximately 9,932 individual bars distributed nationwide are affected.
George J Howe Company, Inc. is recalling 6/11oz Sunflower Seeds Salted due to the presence of undeclared cashew (a tree nut allergen).
Spring & Mulberry Inc. is recalling Spring & Mulberry Lavender Rose Date-Sweetened Chocolate bars due to potential Salmonella contamination. The recall affects multiple batch lots distributed nationwide.
Spring & Mulberry Inc. is recalling Blood Orange Date-Sweetened Chocolate bars due to potential Salmonella contamination. Affected products were distributed nationwide.
Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes used in surgical procedures. The manufacturer identified unapproved design changes to the products that were not cleared by the FDA through the 510(k) process.
Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA clearance. The recall affects 113,843 kits distributed nationwide and in Barbados.
Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside FDA-cleared specifications.
CareFusion 213, LLC is recalling ChloraPrep One-Step (chlorhexidine gluconate and isopropyl alcohol) due to wrinkles in the paper lidding that may breach the seal, compromising sterility assurance.
Medline Industries is recalling four models of Convenience Kits containing Lidocaine and Bupivacaine injections due to quality issues identified during an FDA inspection of the supplier.