State
73,817 recalls have nationwide distribution and so reach Missouri. 8,501 additional recalls listed Missouri specifically in their distribution scope.
Of the 8,501 recalls naming Missouri we have scored against our rubric, 1,339 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,204 (26%) are Severe.
Which agencies issued them
These figures cover only the 8,501 recalls whose distribution notice names Missouri specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Command Electronics is recalling specific LED ceiling lights installed in Jayco and Highland Ridge recreational vehicles because they may produce excessive heat, increasing the risk of a fire.
Heartland is recalling 2018 Pioneer recreational trailers because the liquid propane hose may not be secured, allowing the tire to rub through it and cause a leak.
Forest River is recalling 2018 Prime Time recreational trailers because the Federal Placard lists an incorrect Gross Axle Weight Rating, which could lead to axle failure.
Forest River is recalling 2018 Dynamax, Forester, Sunseeker, and Coachmen Prism vehicles because B-pillar tire labels list pressures that are too low.
Blue Bird is recalling 2015-2019 Vision and 2016 All American school buses because unpadded seat studs may cause head injuries in rear crashes.
Tiny Idahomes is recalling 2014-2017 RVs and trailers because the Federal Placard may display an incorrect Gross Vehicle Weight Rating (GVWR). Owners will receive corrected labels by mail.
Cook Medical is recalling Zenith Alpha Thoracic Endovascular Grafts due to reports of graft thrombosis and occlusion, including one patient death.
Cantrell Drug Company is recalling 21,080 syringes of Glycopyrrolate Injection Solution due to a lack of sterility assurance.
Cantrell Drug Company is recalling Diltiazem HCl 125 mg in 5% Dextrose single-dose bags because of a lack of sterility assurance. The recall covers 2,761 bags distributed nationwide.
Cantrell Drug Company is recalling 1,718 bags of Norepinephrine Bitartrate 16 mg in 0.9% Sodium Chloride 250 mL due to a lack of sterility assurance.
Cantrell Drug Company is recalling 3,039 bags of Norepinephrine Bitartrate 4 mg in 0.9% Sodium Chloride due to a lack of sterility assurance.
Cantrell Drug Company is recalling specific lots of Rocuronium Bromide Injection Solution due to a lack of sterility assurance. The affected syringes were distributed nationwide in the US.
Cantrell Drug Company is recalling specific lots of Glycopyrrolate Injection Solution due to a lack of sterility assurance. The affected syringes were distributed nationwide.
Cantrell Drug Company is recalling Adenosine in 0.9% Sodium Chloride syringes due to a lack of sterility assurance.
Cantrell Drug Company is recalling 8,928 bags of Norepinephrine Bitartrate 8 mg in 0.9% Sodium Chloride 250 mL due to a lack of sterility assurance.
Cantrell Drug Company is recalling 75,840 syringes of Glycopyrrolate Injection Solution nationwide because of a lack of sterility assurance.
Volkswagen is recalling 2006-2016 CC, Passat, and Passat Wagon vehicles because a fuel pump control module defect may cause the engine to stall, increasing crash risk.
Garden of Light Inc. is recalling Woodstock Organic Matcha Vanilla Oats due to potential Listeria contamination. Consumers should check lot codes and stop eating the product.
Cantrell Drug Company is recalling specific lots of Succinylcholine Chloride Injection Solution due to a lack of sterility assurance.
Hospira is recalling 14,300 vials of Hydromorphone Hydrochloride Injection due to the presence of silicone oil particulate matter.
Cantrell Drug Company is recalling specific lots of Phenylephrine HCL syringes because they may lack sterility assurance. The affected products were distributed nationwide.
Cantrell Drug Company is recalling specific lots of Succinylcholine Chloride Injection Solution due to a lack of sterility assurance.
Cantrell Drug Company is recalling specific lots of Sodium Bicarbonate 8.4% Injection Solution because of a lack of sterility assurance.
Cantrell Drug Company is recalling Ephedrine Sulfate syringes due to a lack of sterility assurance. The recall covers 49,666 syringes distributed nationwide.
Cantrell Drug Company is recalling Ephedrine Sulfate in 0.9% Sodium Chloride single-dose syringes because of a lack of sterility assurance.