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 Nov 30, 2016
Merge RadSuite,f/k/a: Emageon Advanced Visualization , RadSuite versions 8.30.7.8, 8.30.7.9, 8.30.8, and 8.31. Advanced…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2016
Philips Healthcare System X-ray Tomography Computed :
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 30, 2016
Blue Bunny Ice Cream Hoppin' Holidoodle ice cream 46 fl. oz. UPC 070640014644 and UPC 070640014651 (high altitude).
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wells Enterprises, Inc.
FDA (openFDA food enforcement)
Reported Nov 23, 2016
Frozen Onion Rings sold and distributed under the following private label retail brands: 1) Premium Pick 5 Mix and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.McCain Foods USA
FDA (openFDA food enforcement)
Reported Nov 23, 2016
MEVION S250 Product Usage: Proton Radiation Therapy
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mevion Medical Systems, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 23, 2016
Version 1.2.0 of Accu-Chek Connect Diabetes Management App (iOS) released on July 11, 2016
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diabetes Care, Inc.
FDA (openFDA device enforcement)
Reported Nov 23, 2016
RF MultiGen¿, 0406-900-000; Refurb RF MultiGen¿, 0406-900-000U
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Nov 22, 2016
Omni Custom Meats, Inc Recalls Roasted Chicken Quarters Due To Misbranding and Undeclared Allergens
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Omni Custom Meats, Inc.
USDA FSIS
Reported Nov 18, 2016
Wayne Farms, LLC Retira Productos De Pechuga De Pollo Listos Para Comer Los Cuales Podran Estar Medios Crudos
High riskUsing this product could cause serious injury, illness or death — stop using it now.Recalling firm not stated
USDA FSIS
Reported Nov 16, 2016
AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove Clip Product is used for the occlusion of the heart's…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AtriCure, Inc.
FDA (openFDA device enforcement)
Reported Nov 16, 2016
X-Force Nephrostomy Balloon Dilation Catheter Kit with Inflation Device, PTFE Sheath, 8 mm x 15 cm, Product Code 996081…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Nov 16, 2016
White Wine & Garlic Wine Drizzle, packaged in 5 oz and 8 oz glass bottles, www.winedrizzle.com, Higginsville, MO 64037
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Get Drizzled Custom Wine Drizzle, LLC
FDA (openFDA food enforcement)
Reported Nov 16, 2016
Accessory Adapter Part number 600525A0 Product Usage: designed for the mounting of MAQUET accessories with the dovetail…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Medical Systems USA
FDA (openFDA device enforcement)
Reported Nov 16, 2016
ReShape Integrated Dual Balloon System, Gen 1, Model No. 01-0013-001, Catalog No. RSM110 product Usage: The ReShape…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Reshape Medical Inc.
FDA (openFDA device enforcement)
Reported Nov 16, 2016
The surgical table is a stand alone unit. Three (3) floor locking cylinders are attached to the base of the surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Schaerer Medical USA Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 16, 2016
FindrWIRZ Guidewire System Catalog# 40-05 Cardiology: The system is intended for use in the cardiovascular system for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.SentreHeart Inc.
FDA (openFDA device enforcement)
Reported Nov 16, 2016
Reprocessed Daig Steerable and Daig Supreme Fixed Curve Diagnostic Electrophysiology Catheters Model Numbers: 401940,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
FDA (openFDA device enforcement)
Reported Nov 16, 2016
Zimmer¿ Air Dermatome II Handpiece Loaner, item number 01-8851-001-00. Device is packaged inside of a padded-foam…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Surgical Inc.
FDA (openFDA device enforcement)
Reported Nov 12, 2016
Schnuck Markets Inc. Recalls Ready-To-Eat Chicken Breast Products That May Be Undercooked
High riskUsing this product could cause serious injury, illness or death — stop using it now.Schnuck Markets, Inc. SLNP
USDA FSIS
Reported Nov 9, 2016
Rigid Suction Canister 3000 CC and 2000 CC.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
FDA (openFDA device enforcement)
Reported Nov 2, 2016
BRACH'S Chocolate Creations, Milk Chocolate Almond Supremes, Fresh roasted almonds drenched in rich creamy milk…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ferrara Candy Comp
FDA (openFDA food enforcement)
Reported Nov 2, 2016
4205 Journey Rolling Walker Product Usage: used to assist people in walking
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nova Ortho-Med Inc.
FDA (openFDA device enforcement)
Reported Nov 2, 2016
VIA 27 Microcatheter, Part No. FG27-154-01, Model No. VIA-27-154-01 The VIA 27 is intended for the introduction of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sequent Medical Inc.
FDA (openFDA device enforcement)
Reported Nov 2, 2016
ex-TEM Assay for ROTEM delta Thromboelastometry System. Art. no.: 503-05 US, ex-tem. Used to monitor the coagulation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TEM Systems Inc.
FDA (openFDA device enforcement)
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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.