State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Frito-Lay is recalling 20-count Bold Mix Sacks nationwide due to the potential presence of Salmonella.
Jimmy's Cookies is recalling The Bakery Peanut Butter Chocolate Chunk Cookies because they may contain undeclared milk. The product was distributed nationwide.
Frito-Lay is recalling Jalapeño Flavored Lays Kettle Cooked and Miss Vickies Kettle Cooked potato chips due to a potential presence of Salmonella.
Frito-Lay is recalling 30-count Miss Vickies Multipack Trays nationwide and in Puerto Rico due to the potential presence of Salmonella.
Arthrex, Inc. is recalling specific Anthrex PEEK SwiveLock SP Vented anchors because some eyelets broke during insertion. The recall covers units distributed in the US and several international locations.
Arthrex is recalling specific SpeedBridge Implant Systems because some eyelets broke during insertion. The recall covers multiple batches distributed in the US and internationally.
Mederi Therapeutics is recalling 1,458 Stretta Catheter kits because a breach in the sterile barrier package compromised sterility.
Isuzu is recalling certain 2008-2009 and 2012-2013 NPR, NPR HD, and GMC W3500/W4500 trucks because the throttle pedal may get stuck, causing high speeds and crash risk.
Zimmer Biomet is recalling 8,154 Regenerex Series A Patella implants because the pegs may shear after surgery.
Reser's Fine Foods is recalling American Classics Macaroni Salad because it contains undeclared milk and soy. The product was distributed to wholesalers in 12 states.
Frito-Lay is recalling 12-count Lays Kettle Cooked Multipacks nationwide due to potential Salmonella presence.
Arthrex, Inc. is recalling specific Anthrex PEEK SwiveLock SP Vented anchors because some eyelets broke during insertion.
Stryker is recalling 119 Medi-Therm Hyper/Hypothermia Systems because the water may reheat too quickly under specific operating conditions.
Roche Diagnostics is recalling 3,946 sample probes for cobas analyzers because corrosion on electrical contacts can disrupt liquid level detection, potentially causing sample carryover.
Teva Pharmaceuticals is recalling specific lots of Clozapine Tablets USP, 25 mg, due to microbial contamination of non-sterile products.
Pinnacle Foods is recalling Great Value Bread and Butter Chips because glass fragments were found in the product. The chips were distributed nationwide.
Arthrex, Inc. is recalling the Anthrex SpeedBridge Implant System because some eyelets broke from the SwiveLock Anchor during insertion.
Treehouse Foods is recalling specific brands of microwaveable macaroni and cheese cups because they may be contaminated with Salmonella.
Douglas is recalling Oliver, Chewie, and Charlotte plush toys because plastic eyes can detach, posing a choking hazard to young children.
Bison Coach is recalling 2016-2018 horse trailers due to incorrect Gross Axle Weight Rating labels, which may lead to overloading and increased crash risk.
Cabrinha is recalling about 2,900 kiteboard control systems because a stainless steel component can break, causing loss of kite control and posing injury and fall hazards.
Arthrex, Inc. is recalling specific Bio-SwiveLock SP Vented anchors because some eyelets broke during insertion.
Arthrex is recalling specific batches of Bio Composite SwiveLock anchors because some eyelets broke during insertion.
Siemens is recalling 159 RAPIDPoint 500 Blood Gas Analyzers because a blank patient ID field may cause demographic errors.
PAR Sterile Products LLC is recalling Buprenorphine Hydrochloride Injection due to the presence of white, crystalline particulates in the vials.