State
72,969 recalls have nationwide distribution and so reach Missouri. 8,465 additional recalls listed Missouri specifically in their distribution scope.
Of the 8,465 recalls naming Missouri we have scored against our rubric, 1,334 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,870 (22%) are Severe.
Which agencies issued them
These figures cover only the 8,465 recalls whose distribution notice names Missouri specifically. The 72,969 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Jaguar Land Rover is recalling 2020–2025 Range Rover Evoque vehicles because the passenger air bag may tear during deployment, reducing occupant protection and risking burn injury from escaping gases.
Jeriflyer 8-inch pool drain covers sold on Amazon do not meet federal safety standards and pose a risk of serious injury or death from entrapment. Consumers should immediately stop using affected pools and contact the seller for a refund.
Autocar is recalling certain 2015-2022 Xspotter and Xpeditor vehicles with insufficient air in their brake system tanks. The defect can reduce brake function and increase stopping distance.
DEWALT has recalled approximately 17,680 Elite Series 40G T27 High Density Flap Discs because the ceramic cloth abrasive flaps can detach during use, causing laceration and injury. Three reports of the flaps detaching resulted in cuts and scrapes.
Trane U.S. Inc. recalls about 4,790 Gas/Electric Packaged Units because the fuel gas valve can open unexpectedly, causing a gas leak and fire hazard. No injuries have been reported.
509 helmets and 509 for Polaris helmets may fail to provide sufficient protection in a crash. One incident reported a helmet detachment during a crash resulting in a concussion.
SNLN Party Supply Toys containing button cell batteries are being recalled because the battery compartments can be easily opened by children, posing a risk of serious injury or death if swallowed.
Harbor Freight Tools is recalling about 6,500 Predator 2000-Watt Power Stations due to reversed wires in the AC outlet receptacles when in Emergency Power Supply mode, creating a shock hazard to consumers.
Positec is recalling about 49,000 Hyper Tough, Worx, and Portland brand electric corded chainsaws and pole saws due to a defective main switch that can fail and allow the saws to continue running, posing a laceration hazard.
NHTSA is recalling 2025 Can-Am Canyon motorcycles because a drive belt support may fail, causing loss of power and increasing crash risk.
Autocar is recalling 2012-2025 Xspotter vehicles because incorrect tire inflation labels may lead to under-inflated tires, increasing crash risk.
Kraft Heinz is recalling Oscar Mayer Turkey Bacon products nationwide due to possible Listeria monocytogenes contamination. No illnesses have been reported.
Fresenius Medical Care is recalling 0.9% Sodium Chloride Injection in flexible plastic containers nationwide due to lack of assurance of sterility. The FDA classified this as a Class II recall.
Thrive Health and Wellness, LLC is recalling LL Bioboost Injectable pre-filled syringes nationwide due to lack of assurance of sterility. The affected product is Lot #H277639 with expiration 6/25/2025.
Integra LifeSciences is recalling Extended Tip Applicator 8CM devices nationwide and internationally because they may contain potentially out-of-specification endotoxin levels and lack sterility assurance.
Thrive Health Solutions is recalling Semaglutide 2.5 mg/mL pre-filled syringes (Lot #H270221) because the manufacturer cannot assure sterility of the product.
Thrive Health Solutions is recalling Methylcobalamin Injectable 10mg/mL pre-filled syringes (Lot #H228307, expiration 12/27/2025) due to lack of assurance of sterility. The affected product was distributed nationwide.
Thrive Health Solutions is recalling LX Bioboost Plus pre-filled syringes due to lack of assurance of sterility. The affected product is a multi-ingredient injectable formulation distributed nationwide.
Apotex Corp. is recalling Ketorolac Tromethamine Ophthalmic Solution 0.5% due to lack of assurance of sterility. The recall affects 87,840 bottles distributed nationwide.
Thrive Health Solutions is recalling one lot of Tirzepatide/Cyanocobalamin Injectable pre-filled syringes due to lack of assurance of sterility. The affected product is Lot C03125A distributed nationwide.
Thrive Health Solutions is recalling Tirzepatide Injections 30mg/mL pre-filled syringes due to lack of assurance of sterility. The affected product was distributed nationwide.
SunMed Holdings is recalling Broselow Pediatric Emergency Rainbow Tape due to incorrect values printed on the tape that could lead to improper medication dosing and defibrillation in pediatric emergency care.
B Braun Medical Inc. is recalling 187,656 containers of 0.9% Sodium Chloride Injection USP due to potential sterility failures caused by pinholes in finger boxes during manufacturing. The defect may allow leaks and compromise the sterile nature of the intravenous medication.
Becton Dickinson is recalling BD BACTEC MGIT 960 PZA Kit due to reports of intermittent false resistance results during pyrazinamide susceptibility testing of Mycobacterium tuberculosis. The issue affects units distributed worldwide.
Thrive Health Solutions is recalling Semaglutide 5 mg/mL pre-filled syringes distributed nationwide because the manufacturer cannot assure the product's sterility.