Recalls distributed in Missouri
These notices name Missouri in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
4,082 stored notices name Missouri, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Missouri too — those are in the archive.
Reported Apr 5, 2023
ISH Shrimpish Sample Meal Kit: ( Sample Meal Kit ) a package containing two ISH Foods plant-based Shrimpish products…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Ish Company
FDA (openFDA food enforcement)
Reported Mar 29, 2023
BD Pyxis Anesthesia ES System (PAS ES), REF: 327; BP Pyxis MedStation ES (Med ES Main), REF: 323; BD Pyxis MedStation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Mar 29, 2023
DeRoyal SafeLiner Suction Canister, 1000cc, REF PHESL-1000B
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DeRoyal Industries Inc.
FDA (openFDA device enforcement)
Reported Mar 29, 2023
DG Health brand Sugar Free Daily Fiber in 10 oz. plastic containers (UPC: 860005934294).
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Dollar General Corporation
FDA (openFDA food enforcement)
Reported Mar 29, 2023
Russel Stover Sugar Free Peanut Butter Cups packaged in 2.4oz peg bag, containing individually wrapped pieces. UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Russell Stover Candies Inc.
FDA (openFDA food enforcement)
Reported Mar 22, 2023
Egg roll wrappers, 6" x 6" and 7" x 7", packaged in 30lb. corrugated (cardboard) boxes. Product is sold frozen.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Baily International Foods
2 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 22, 2023
Bard Mission Disposable Core Biopsy Instrument Kit: 16G x 10CM, REF: 1610MSK; 18G x 16CM, REF: 1816MSK
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Mar 22, 2023
Brainlab ExacTrac Dynamic software, Medical Charged-Particle Radiation Therapy System, model 20910-01E and 20910-01F.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Mar 22, 2023
Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-cup pods; packed 24 to a box
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Keurig Dr Pepper
FDA (openFDA food enforcement)
Reported Mar 22, 2023
Fusion Bioline Vascular Graft, Part number M00201503046B0
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Cardiovascular, LLC
FDA (openFDA device enforcement)
Reported Mar 22, 2023
ENFAMIL PROSOBEE PWD 12.9OZ (6CAN) US
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mead Johnson & Company
FDA (openFDA food enforcement)
Reported Mar 22, 2023
Sunflower Lecithin Powder Packaged in 44 lb. (20 kg.) boxes
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Navada Imports
3 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 15, 2023
Brussel Sprouts 98.5% of product was packaged for retail and 110 cases were bulk Brands: 4 Earth Farms, Trader Joe s,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.4 Earth Farms formerly Mcl Fresh Inc.
FDA (openFDA food enforcement)
Reported Mar 15, 2023
Simplexa COVID-19 Direct, REF: MOL4150; including Reaction Mix, REF: MOL4150; with previous assay definition v2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DiaSorin Molecular LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 15, 2023
Given Imaging SmartBar Cereal Bar; Net Weight 2.53 oz (72 g); Ingredients: glucose syrup, soy crisps, oats, pea…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Given Imaging Ltd.
FDA (openFDA food enforcement)
Reported Mar 15, 2023
PREAT NOBIL GRIP, product numbers 0102000 and 01202000-3 (3 pack), 5-ml vials packaged in pouches, dental anaerobic…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Preat Corp.
FDA (openFDA device enforcement)
Reported Mar 8, 2023
HEILEMANN CONFISERIE WEHNACHTSFIGUREN AUS EDELVOLLMILCH-SCHOKOLADE Solid Chocolate Holiday Treats 3.5 oz box UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alpenland International, Inc.
FDA (openFDA food enforcement)
Reported Mar 8, 2023
Alaris PC Unit 8015 utilizing 802.11 b/g or 802.11 a/b/g wireless network cards, with IP addresses from x.x.x.224 to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Feb 15, 2023
The Covera Vascular Covered Stent is a flexible, self-expanding endoprothesis comprised of ePTFE encapsulating a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Feb 15, 2023
RipCord Syndesmosis Button, REF: STA001K
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TriMed Inc.
FDA (openFDA device enforcement)
Reported Feb 8, 2023
Catalog Number / Product Description 0601600 2.7F Broviac CV Catheter Repair Kit 0601610 4.2 Fr Broviac CV Catheter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Feb 8, 2023
AxiEM" Non-Invasive Patient Tracker
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Feb 8, 2023
SynCardia Total Artificial Heart System (70CC): 500101-001 SynCardia Total Artificial Heart System (50CC): 570500-000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SynCardia Systems LLC
FDA (openFDA device enforcement)
Reported Feb 8, 2023
GORE CARDIOFORM Septal Occluder, REF: GSX0030A
Moderate riskThis product could cause temporary or reversible health problems — stop using it.W L Gore & Associates, Inc.
FDA (openFDA device enforcement)
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Other states
RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.