State
73,596 recalls have nationwide distribution and so reach Missouri. 8,496 additional recalls listed Missouri specifically in their distribution scope.
Of the 8,496 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 2,203 (26%) are Severe.
Which agencies issued them
These figures cover only the 8,496 recalls whose distribution notice names Missouri specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Zavation's ZVplasty System surgical devices may not have been adequately sterilized, creating infection risk. The recall affects 195 units distributed nationwide in the US across multiple lot numbers.
Clio LLC is recalling Clio No Added Sugar Yogurt Bars (Mixed Berry/Peach, 50g) due to possible metal fragments in the product. Approximately 1,880 units were distributed nationwide.
Zavation is recalling ZVplasty 10G spinal implant kits that may not have been properly sterilized. The affected devices were distributed nationwide and may pose infection risk if implanted.
Clio LLC is recalling Clio Greek Yogurt Bar Vanilla/Strawberry Club pack 50g x 12, 16pc tray due to possible metal fragments in the product. Consumers should not consume the affected product.
Oxford Pharmaceuticals is recalling 6,864 bottles of Buspirone Hydrochloride Tablets, 15 mg, distributed nationwide due to the presence of foreign tablets or capsules in the product.
A cooling unit in the Philips BRILLIANCE VOLUME computed tomography system may unexpectedly eject from the gantry, posing a risk of injury. Two affected units are being recalled.
Zavation is recalling 56 units of 10 gauge direct unilateral stylets used in spinal procedures because products distributed as sterile may not have been adequately sterilized. Affected units were distributed nationwide.
Zavation is recalling 7 units of 11G DIRECT SINGLE spinal implants (lots 2001185 and 2001243) because products distributed as sterile may not have been adequately sterilized. The devices were distributed nationwide.
Zavation's 10G Direct Single Bone Access Kits are being recalled because products distributed as sterile may not have been adequately sterilized, posing infection risk in orthopedic procedures.
A software defect in Change Healthcare Enterprise Viewer versions 2.0 and 2.1 prevents the display of image presentation styles. The viewer is used nationwide for displaying medical images.
Genpak is recalling Bake n Show Muffin Trays in three sizes due to the discovery of foreign objects in product packaging. The recall affects units distributed across multiple US states and Canada.
Genpak is recalling Bake n Show Round and Square Cake Trays due to the presence of foreign objects found in product packaging. The trays were distributed across multiple U.S. states and Canada.
Hi Tech Pharmaceuticals is recalling Lipodrene With 25mg Ephedra Extract because the product contains 1,4-dimethylamylamine (DMAA), an unapproved food additive.
K2M, Inc is recalling Cascadia AN Interbody Convex lumbar implants with mislabeled product dimensions. The affected sizes include 10x22x14mm, 10x28x14mm, and 10x22x15mm. No injuries have been reported.
Genpak is recalling Bake n Show Oven Ready Food Trays (16 ounce) due to foreign objects found in the packaging. The affected product was distributed across multiple U.S. states and Canada.
Genpak is recalling Bake n Show Angel Food Trays (8-inch and 8-inch shallow models) because foreign objects were found in the product packaging. Consumers should stop using affected trays.
Genpak is recalling Bake n Show Pizza Cookie Trays (12") because foreign objects were found in product packaging. The recall affects multiple states and Canada.
Mylan Institutional LLC is recalling Thiamine Hydrochloride Injection USP 200 mg/2 mL due to vials labeled with incorrect lot numbers. The cartons contain the correct lot number 200906 but vials inside are labeled with lot number 200901.
Jaguar Land Rover is recalling 2020-2022 Defender X vehicles with smoked rear lights because a voltage spike can cause turn signals and brake lights to fail.
One More Auto Parts is recalling Lasfit headlight bulbs that are too bright during the first ten minutes of use, posing a crash risk.
Coach House is recalling 2021 Platinum vehicles because an overtightened bolt on the cooking stove may damage the seal, causing a gas leak that increases fire risk.
Honda is recalling 2022 Odyssey vehicles because second-row outboard seat frames have deformed locking mechanisms that may prevent them from locking into place. Unlocked seats could move unexpectedly, increasing injury risk.
Highland Ridge RV is recalling certain 2019-2021 fifth wheel and travel trailers because a propane regulator may fail, increasing fire risk.
KZRV is recalling 2018-2019 Sidewinder RVs because a propane regulator may fail, increasing pressure and fire risk.
Jayco is recalling approximately 87,649 certain 2017-2021 travel trailers and fifth wheels with defective Winntec propane regulators that may fail and increase fire risk.