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.
Honda is recalling 2026 Pilot and Passport vehicles because improperly tightened rear subframe bolts may lead to vehicle instability or detachment, increasing crash risk.
Spring & Mulberry Inc. is recalling Pure Dark and Pure Dark Minis date-sweetened chocolate products nationwide due to potential Salmonella contamination. Consumers should not consume the affected products and should discard or return them.
BMW is recalling 428 vehicles from 2023-2025 due to a potential integrated brake system malfunction that may reduce braking power or disable stability controls.
George J Howe Company, Inc. is recalling 5# Sunflower Seeds C/S due to the presence of undeclared cashew, a tree nut allergen. The product was distributed across multiple U.S. states.
Spring & Mulberry Inc. is recalling Blood Orange Date-Sweetened Chocolate bars due to potential Salmonella contamination. Affected products were distributed nationwide.
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.
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.
Intuitive Surgical recalls certain Da Vinci surgical system operative components due to a defective E-brake retainer pin that may fail to engage the E-brake, potentially causing uncontrolled motion and patient injury.
CareFusion is recalling 178,000 ChloraPrep One-Step antiseptic applicators (Lot #4073005) nationwide due to potential non-sterility from fungal contamination and seal breaches from paper lidding wrinkles.
George J Howe Company is recalling 5# Sunflower Seeds C/NS due to the presence of undeclared cashew, a tree nut allergen. The product was distributed across 24 states.
Abiomed is recalling certain Impella CP Set with SmartAssist (10th Generation) units with affected 14Fr Low Profile Introducer Kits due to potential for thrombus (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.
Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA clearance.
Surgify Medical is recalling Surgify Halo 4.0 mm Extendable surgical burrs due to potential breakage during bi-portal endoscopic spinal surgery. The breakage could create a safety hazard during the procedure.
Ventec Life Systems is recalling VOCSN+Pro respiratory systems due to a damaged backup battery that may prevent the backup alarm from activating during power loss, delaying caregiver awareness of a hazardous condition.
Spring & Mulberry Inc. is recalling Spring & Mulberry Coffee Date-Sweetened Chocolate bars due to potential Salmonella contamination. The affected product was distributed nationwide.
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.
Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside FDA-cleared specifications. The recall affects approximately 113,843 kits distributed nationwide.
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.
Prime Food Processing LLC. is recalling 69 cases of Dried Herring Fish 7 oz. due to improper evisceration that may allow Clostridium botulinum contamination.
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.
Medline Industries is recalling Medline Convenience Kits (models DYNJ905503F and DYNJ905503G) that contain Arrow Kits with Lidocaine Hydrochloride Injection and Bupivacaine Hydrochloride in Dextrose Injection due to quality issues found during an FDA inspection of the supplier.
George J Howe Company is recalling 6/11oz No Salt Sunflower Seeds due to the presence of undeclared cashew, a tree nut allergen. The product was distributed across 24 U.S. states.
Spring & Mulberry Inc. is recalling Spring & Mulberry Mixed Berry Date-Sweetened Chocolate bars due to potential Salmonella contamination. The recall affects approximately 66,779 individual bars distributed nationwide.
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.