State
73,100 recalls have nationwide distribution and so reach Missouri. 8,493 additional recalls listed Missouri specifically in their distribution scope.
Of the 8,493 recalls naming Missouri we have scored against our rubric, 1,344 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,882 (22%) are Severe.
Which agencies issued them
These figures cover only the 8,493 recalls whose distribution notice names Missouri specifically. The 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Toyota is recalling certain 2024 Lexus RX and 2024-2025 NX vehicles because driver and front passenger head restraints may be removed inadvertently without pressing the lock release, failing FMVSS 202.
Micro Bird is recalling 22,582 school buses because the rear emergency door handle may break, potentially delaying emergency access.
Kido Sports is recalling Scorpion EXO Covert X and Harley-Davidson HD-X07 helmets because they may not stay securely fastened, increasing injury risk.
REI is recalling Co-op Cycles REV children's bicycles (12-, 16-, and 20-inch models, 2022-2024) because the training wheel assembly knob can loosen and detach, creating fall and injury hazards.
At Home Procurement is recalling approximately 990 Tie Dye Fur Toy Trunk Storage Chests sold from September 2023 through February 2024 because they lack a lid support feature and ventilation holes, creating entrapment and suffocation hazards.
Micro Bird is recalling 794 transit buses because the rear emergency door handle may break, potentially delaying emergency access.
GM is recalling certain 2020-2022 Bolt EV and 2022 Bolt EUV vehicles previously remedied under 21V-650, because diagnostic software may have been installed incorrectly and fail to detect defective battery modules.
Daikin Comfort Technologies is recalling about 56,000 Daikin FIT, Amana Brand S-series, and Goodman SD heat pumps due to a power interruption defect that can cause the units to provide heat even when the thermostat is set to cooling mode, posing a risk of excessive heat exposure.
ZOLL is recalling operator's guides for the ZOLL 731 Ventilator because they omit critical MRI safety information. Missing distance guidance could cause the ventilator to malfunction during MRI procedures.
Hamilton Medical AG is recalling the HAMILTON-C6 ventilator due to a sensor failure that may prevent re-initiation after reconnection, potentially causing hypoxia.
Nissan is recalling 2024 Frontier vehicles because an oversized ball joint may separate, causing loss of steering control and increasing crash risk.
OSSOS-SANS Reforzado tablets are being recalled because they contain undeclared active pharmaceutical ingredients—diclofenac and methocarbamol—and were marketed without FDA approval.
Outset Medical is recalling 431 TabloCart hemodialysis system carts due to power cord connector defects that may cause overheating, sparks, and smoke, potentially delaying treatment or causing burns.
Daimler Trucks North America is recalling 162 Thomas Built Buses Saf-T-Liner C2 and C2 Jouley school buses because the emergency exit alarm may not sound.
Ethicon recalled 287,892 MONOCRYL Plus Antibacterial Sutures worldwide due to a packaging machine defect that created holes in primary packaging, potentially compromising sterility and risking infection.
Breckenridge Pharmaceutical recalls Duloxetine 60mg capsules nationwide due to N-nitroso-duloxetine impurity levels exceeding FDA interim limits. Affected lots had current good manufacturing practice (CGMP) deviations.
C.R. Bard Inc is recalling 6,420 Foley catheter trays nationwide because some devices may not display temperature readings or may display erratic readings. The malfunction could affect patient monitoring.
Teva Pharmaceuticals is recalling 34,448 bottles of Amoxicillin and Clavulanate Potassium Tablets USP (Chewable 400mg/57mg) distributed nationwide due to subpotency. The recall is voluntary and initiated by the firm.
Ethicon recalls 341,532 units of VICRYL surgical sutures worldwide due to holes in primary packaging that compromise sterility and could result in infection.
Lupin Pharmaceuticals is recalling one lot of Cefixime oral suspension (200 mg/5 mL) due to failed content uniformity specifications. The recall affects 3,552 bottles distributed nationwide.
Beaver Visitec International is recalling the Xstar Safety Slit Knife Model 378227 because some units have the blade bevel installed incorrectly—facing downward instead of the intended upward orientation.
Howmedica is recalling the Gray Revision Instrument System Accessory Tray/Case due to a design flaw that may enable reuse and re-sterilization of single-use, sterile-packaged instruments.
Ethicon is recalling 56,952 units of PDS II polydioxanone sutures distributed worldwide because a packaging defect resulted in compromised sterility, which could lead to infection. No illnesses have been reported.
Consumer Product Partners is recalling Pure Petroleum white petrolatum products sold at Rite Aid, Kroger, Harris Teeter, and CVS nationwide because the products labeled as pure white petrolatum actually contain undisclosed lavender and chamomile.
Baxter Healthcare is recalling Centrella Max and Pro+ hospital bed mattresses that may develop delaminated top covers when cleaned with bleach-containing solutions. The mattresses prevent and treat pressure injuries.