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 48,123 notices were distributed nationwide, so they reach Missouri too — those are in the archive.
Reported Jul 22, 2015
Diet Bubba Cola, 20 FL. OZ (1.25 PT) 591 mL INGREDIENTS: CARBONATED WATER, HIGH FRUCTOSE CORN SYRUP, CARAMEL COLOR,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Dr. Pepper Snapple Group Inc.
FDA (openFDA food enforcement)
Reported Jul 22, 2015
MOSAIQ Oncology Information System MOSAIQ is an oncology information system used to manage workflows for treatment…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jul 22, 2015
Dual Delivery 4DD-1 of GYC-1000 Green Laser Photocoagulator system GYC4DD-1: The Nidek Green Laser Photocoagulator…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nidek Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 22, 2015
0210-312-000-Woundcare Replacement kit with soft tip; 0210-318-000; Woundcare Replacement with fan tip; 0210-318-100-…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Jul 22, 2015
16mm Chisel Blade; used in the LCP Anterior Ankle Arthodesis Plate System and the Hip Preservation Surgery Set.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 22, 2015
Patient Handling System (Motion Control Software), Product Usage: Indicated for stereotactic radiosurgery and precision…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Viewray Incorporated
FDA (openFDA device enforcement)
Reported Jul 22, 2015
Natural Grocers Caribbean Fruit & Nut Mix, Net Wt. (10 oz) (283g), packaged in plastic bag.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vitamin Cottage Natural Food Markets, Inc.
FDA (openFDA food enforcement)
Reported Jul 15, 2015
Natrelle Re-sterilizable Breast Implant Sizer, Size: 410 cc, Style No. MSZFX410. The product is packaged in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Allergan Inc.
FDA (openFDA device enforcement)
Reported Jul 15, 2015
Foil bags containing 2.2 lbs. each of almond flavored powder and sold under the Boba Direct, Inc. brand.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boba Direct, Inc.
23 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 15, 2015
Breast Pack - contains Devon Light Glove Used during surgery
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stradis Healthcare, LLC.
50 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 15, 2015
TITANIUM END CAP WITH T40 STARDRIVE RECESS, 0MM EXTENSION FOR TITANIUM TIBIAL NAILS-EX; Synthes Tibial Nail System EX…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes, Inc.
FDA (openFDA device enforcement)
Reported Jul 8, 2015
Etest Cefotaxime CT 256 WW and Etest Cefotaxime CT 256 US. in vitro diagnostic.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported Jul 8, 2015
HeartWare Ventricular Assist System (HVAD) For use as a bridge-to-cardiac transplantation in patient who are at risk of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HeartWare Inc.
FDA (openFDA device enforcement)
Reported Jul 8, 2015
Spine Wave Access Kit, Catalog Number 10-1530 Package contents: RLSP494-Rhythmlink Monopolar Stimulating Probe and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spine Wave, Inc.
FDA (openFDA device enforcement)
Reported Jul 8, 2015
Infinite F500, in vitro diagnostic. Product Usage: The Tecan Infinite F500 is a multifunctional microplate reader with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tecan US, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2015
Treatment Planning and Delivery System Software version 3.6. ViewRay. Indicated for stereotactic radiosurgery and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Viewray Incorporated
FDA (openFDA device enforcement)
Reported Jul 8, 2015
Natural Knee II Revision Femoral Stem, 125mm, item 6215-12-185. packaged in configuration 803/791. Knee Prosthesis…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Jul 1, 2015
The spare component Anti-HBs Cutoff Calibrator, 10 mLU/mL, Catalog number 26154. The spare component is sold separately…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Bio-Rad Laboratories, Inc.
FDA (openFDA device enforcement)
Reported Jul 1, 2015
LapSac Surgical Tissue Pouch. The current intended use for the LapSac Surgical Tissue Pouch is for isolating tissue…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
FDA (openFDA device enforcement)
Reported Jul 1, 2015
McKesson Medi-Pak Vaginal Speculum, 10/bag Reorder No. 11-8309 Used to expose interior of the vagina to facilitate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Jul 1, 2015
Epi breads, 7" French Hoagie Sliced, Net Weight 10.4 lbs., Lavoi Corporation, EPI Breads, 4710 West Ledbetter, Dallas,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lavoi Corporation d/b/a/ Epi De France
21 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 1, 2015
VersaTREK Instrument Series 240 REF 6240, Manufactured for Remel Inc. The VersaTREK System is for cultivating and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 1, 2015
Lifesaver Single Patient Use Manual Resuscitator Product Usage: The Hudson RCI Lifesaver Single Patient Use manual…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Teleflex Medical
FDA (openFDA device enforcement)
Reported Jul 1, 2015
Custom Cardiovascular Procedure Kits; Over-Pressure Safety Valves. For use only in the extracorporeal circuit for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corp.
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.