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 48,122 notices were distributed nationwide, so they reach Missouri too — those are in the archive.
Reported Oct 19, 2018
Caito Foods, LLC Recalls Salad And Bowl Products Made With Chicken Due To Possible Salmonella and Listeria…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Caito Foods, LLC
USDA FSIS
Reported Oct 17, 2018
Codan Filter (Codan catalog number BC 693) used with Medrad Patient Administration Sets (PAS) and Intego PET Infusion…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bayer Medical Care, Inc.
FDA (openFDA device enforcement)
Reported Oct 17, 2018
Colpo-Pneumo Occluder, Part CPO-6
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Oct 17, 2018
NeoMed Enteral Feeding Tubes with Enteral Only Connectors, French sizes 4.0Fr, 5.0Fr, 6.5Fr, 8.0Fr, and lengths 40cm,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Neomed Inc.
FDA (openFDA device enforcement)
Reported Oct 17, 2018
Miso Milo Chocolate (cookies); A Sarap Asian Fusion Product; Net Wt. 70 G/Cookie; Contains: Flour, eggs, Baking Soda,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sarap Asian Fusion
3 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 10, 2018
Laparoscopy Instruments Instructions For Use (IFU) for the following: 1)Monopolar electrode, 2) Insert, handle and/or…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Dannoritzer Medizintechnik GmbH & Co. KG
FDA (openFDA device enforcement)
Reported Oct 10, 2018
ENDOLOGIX AFX Endovascular AAA System, Stent Graft System, Rx Only, Sterile EO, REF: BA22-120/I20-40, BA22-100/I20-40,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Endologix
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 10, 2018
Leica HistoCore SPECTRA CV Coverslipper, used in preparation of histological and cytological tissue samples for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 10, 2018
Crazy About Cookies***GLUTEN FREE CHOCOLATE CHIP COOKIE DOUGH**Net Wt. 2 lbs. (907.18g)**Nutrition facts***Ingredients:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Neighbors LLC
FDA (openFDA food enforcement)
Reported Oct 10, 2018
C-flex 570C +19.0D Intraocular Lens Product Usage: C-flex IOLs are designed to be surgically implanted into the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rayner Intraocular Lenses Limited
FDA (openFDA device enforcement)
Reported Oct 10, 2018
TrueBeam Radiotherapy Delivery System version 2.0 and 2.5 EDGE Radiotherapy Delivery System version 2.0 and 2.5 Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Varian Medical Systems
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 10, 2018
EVERYBURGER - Burger-Shaped Chocolate Cookies: NET WT. 2.32 oz. (66 g) There are 2 packing sizes; 10 items per case and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wismettac Asian Foods (USA) dba Nishimoto Trading Co. Ltd.
FDA (openFDA food enforcement)
Reported Oct 3, 2018
DX-D 600 Product Usage: The DX-D 600 system is a ceiling mounted General Radiography X-Ray imaging system used in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Agfa N.V.
FDA (openFDA device enforcement)
Reported Oct 3, 2018
Bausch + Lomb Stellaris Elite 20 GA Vit Cutter, Model BL5626, 7500 cpm, packaged in sterile pouches, 6/shipper.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bausch & Lomb Inc.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 3, 2018
HipLOC Hip Fracture Fixation System- Hiploc System 130¿ Plate 38 mm Barrel 4 Hole Plate Item Number: 2110-130-004…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet UK Ltd.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 3, 2018
ESSENTIO Pacemaker
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
5 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 3, 2018
Gotham Greens Classic Pesto 6.5 oz. plastic cup, 12 cups per case. Refrigerated. UPC 85392700334
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brett Anthony Foods
FDA (openFDA food enforcement)
Reported Oct 3, 2018
Retractor System Elastic Stays (Part 3314-lG; 3316-lG; 3550-lG) Product Usage: The Retractor System Elastic Stays (Part…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Oct 3, 2018
Discovery MR750w Nuclear Magnetic Resonance Imaging System labeled as the following product name sold under: Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
FDA (openFDA device enforcement)
Reported Oct 3, 2018
Visualase Thermal Therapy System, Software: Visualase Software versions 3.1.1 - 3.2, Product #: 9735542
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Oct 3, 2018
Medtronic Clip Gun Magazines are packaged in individually sealed pouches and distributed in boxes containing 5…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neurosurgery
FDA (openFDA device enforcement)
Reported Oct 3, 2018
INTEGRIS Allura 9, System Code 722018 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
26 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 26, 2018
400mL, Premium, Urine Meter, 16 FR, Silicone Temperature Sensing Foley Traywith Cath-Secure Plus, Sterile, Item Code…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 26, 2018
PR1000 Pivot Rehab Bed AC powered adjustable bed.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Med-Mizer, Inc.
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Missouri recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.