State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ford is recalling 2016 F-150 trucks with Multi-Contour Seats because the passenger air bag sensor may misclassify adults as children, preventing air bag deployment.
Vapor Bus is recalling 4,826 Electric Transit Operator Controller Assemblies due to a software defect that may cause rear bus doors to open unexpectedly while in motion.
Ford is recalling 2015-2016 Transit vans because rear seat belt buckles may fail to latch if damaged by heavy objects, increasing crash injury risk.
Premiere Sales Group is recalling Rhino 7 3000 bottles because they contain undeclared active pharmaceutical ingredients, desmethyl carbondenafil and dapoxetine.
Medisca Inc is recalling L-Citrulline API bottles because FDA testing found the product contained N-acetyl-leucine instead of the labeled ingredient.
MSNV, Inc dba National Video Supply is recalling Rhino 7 Platinum 3000 single blister packs because they contain undeclared active pharmaceutical ingredients.
Nuway Distributors is recalling APEXXX tablets because they contain sildenafil, an unapproved drug for erectile dysfunction.
Life and More LLC is recalling Akttive High Performance Fat Burner Gold capsules because FDA testing found undeclared sibutramine, desmethylsibutramine, and phenolphthalein.
FDA recalls Rhino 7 Platinum 3000 because it contains undeclared active pharmaceutical ingredients, desmethyl carbondenafil and dapoxetine.
Medline Industries is recalling 500 mg acetaminophen tablets mislabeled as 325 mg. Consumers should stop using the product and return it to the retailer.
Inaffit, LLC is recalling Natureal Burn Fat Nature capsules because the product contains undeclared sibutramine and was marketed without an approved NDA or ANDA.
Fit Firm and Fabulous is recalling Ultimate Herbal Slimcap Capsules because they contain undeclared sibutramine, a controlled substance removed from the U.S. market for safety reasons.
Hospira is recalling 213,600 bags of Magnesium Sulfate in Water for Injection because the primary bag labeling may be mislabeled with a barcode that scans as heparin sodium.
MSNV, Inc dba National Video Supply is recalling Rhino 7 3000 bottles because they contain undeclared active pharmaceutical ingredients.
Medtronic is recalling 364,768 Endo GIA Ultra Universal Short Stapler Handles because they may fail to fire or partially fire, and the articulating lever may disengage during use.
General Motors is recalling 2016 Buick Regal vehicles because the power-steering assist system may fail, increasing crash risk.
Medtronic is recalling 2,711 Best Practice Kits containing specific Endo GIA Ultra Universal Stapler Handles due to reports of staplers failing to fire or partially firing, and articulating levers disengaging during use.
Alcon is recalling TEARS Naturale FREE eye drops because some vials may contain water instead of the product, creating a sterility risk.
Medtronic is recalling 1,102,166 Endo GIA Ultra Universal Standard Stapler Handles worldwide because they may fail to fire or partially fire during surgery.
BlendTech Inc is recalling Uncle Buck's Fish Batter Mix Original because it contains an undeclared milk ingredient. The product was distributed nationwide.
Varian Medical Systems is recalling Eclipse Treatment Planning System versions 11, 13.0, 13.5, and 13.6 due to a dose calculation error that may result in unintended radiation exposure.
Campagna is recalling 2013-2015 T-Rex motorcycles because the steering column may disconnect from the steering rack, causing loss of steering control.
Medtronic is recalling 327,797 Endo GIA Ultra Universal 12 mm XL Stapler Handles worldwide because the staplers may fail to fire or the articulating lever may disengage during surgery.
Temsa is recalling 70 model year 2016 TS45 and TS35C buses because front lower control arm housings may crack. This defect could cause a loss of steering and increase the risk of a crash.
Medline Industries is recalling 325 mg acetaminophen tablets that are actually 500 mg due to a labeling error.