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.
Louis Garneau is recalling specific Course bicycle helmets because they do not meet federal impact safety standards, posing a risk of head injury.
Pagani is recalling 2017 Huayra Coupe BC and Roadster vehicles because battery management software may prevent the car from starting or idling, increasing crash risk.
Handi-Craft is recalling Dr. Brown's Lovey pacifier and teether holders because the snap can detach, posing a choking hazard to young children.
eheat is recalling about 35,000 Envi wall heaters sold in the U.S. and Canada due to a defect that can cause overheating, smoke, or melting, posing a burn hazard.
Toyota is recalling 2018 Prius C vehicles sold in Puerto Rico because the front passenger air bag and child seating labels may be missing, increasing crash injury risk.
Lotte International America Corp. is recalling Lotte Kancho Choco-Biscuit products because peanut allergen was found during product sampling and testing.
Ferrara is recalling 2004-2012 Inferno and Igniter emergency vehicles because front axle spindles may crack and fail, potentially causing a wheel to separate.
Apollo Care is recalling 360 bags of Vancomycin IV solution because stability data does not support the assigned 90-day beyond use date.
Kovatch Mobile Equipment is recalling specific KME Predator fire apparatus vehicles because inconsistent machining may cause front axle spindles to crack and fail, potentially leading to wheel separation.
Maserati is recalling 2017 Quattroporte and Ghibli vehicles because an engine software issue may cause the transmission to shift into neutral or the engine to shut off unexpectedly.
Apollo Care is recalling 312 bags of Vancomycin IV solution because stability data does not support the assigned 90-day beyond use date.
Roche Diagnostics is adding a warning to cobas 6000 and 8000 Modular Series Operator Manuals to prevent operator injury during maintenance.
Abbott is recalling ARCHITECT c8000 Cuvette Segments because a detached post can cause falsely depressed patient results on c4000, c8000, and c16000 instruments.
Synthes (USA) Products LLC is recalling 1,144 sterile 2.5 mm Reaming Rods due to potential gaps in the package seal that may compromise sterility.
Heartland Coca-Cola Bottling Company is recalling Sprite Zero cans because sharp edges on the cans could cut consumers' mouths.
Heartland Coca-Cola Bottling Company is recalling Sprite cans due to sharp edges that could cause cuts to consumers' mouths.
Heartland Coca-Cola Bottling Company is recalling Pibb Zero soda cans because sharp edges were observed, posing a risk of cuts to consumers' mouths.
Heartland Coca-Cola Bottling Company is recalling 766,271 cases of Coca-Cola Vanilla Zero 12 oz cans due to sharp edges that may cause mouth cuts.
Abbott Laboratories is recalling cuvette segments for the ARCHITECT Clinical Chemistry system because detached segment posts may cause falsely depressed patient test results.
Medtronic is recalling 449 O-arm O2 Imaging Systems because servicing internal components may cause an electrical short, posing a shock hazard to field service technicians.
Heartland Coca-Cola Bottling Company is recalling Dr Pepper Diet cans because sharp edges were observed, posing a risk of cuts to consumers' mouths.
Mindray is recalling 2,875 A-Series anesthesia delivery systems due to a software issue that may apply incorrect settings or skip startup leak tests.
Synthes (USA) Products LLC is recalling sterile Light Clips for the Oracle Retractor because potential gaps in the package seal may compromise sterility. The product is used during orthopedic surgery.
Mindray is recalling A7 Anesthesia Delivery Systems because a software issue may cause incorrect settings to be applied or the startup leak test to be skipped.
Zimmer Biomet is recalling 127 Sirus Drill instruments because they may not be adequately cleaned, potentially leading to infection.