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 Nov 13, 2019
SPIFE Alkaline Hemoglobin Kit, Cat. No. 3415, for use in the separation and quantitation of hemoglobins by agarose…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Helena Laboratories, Corp.
FDA (openFDA device enforcement)
Reported Nov 13, 2019
The LivaNova VNS Therapy System, used for Vagus Nerve Stimulation (VNS), consists of an implantable VNS Therapy…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Autoject EI, REF AJ1310
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Owen Mumford USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2019
SCFE (slipped capital femoral epiphysis) Knobs for Driver, 6.5mm and 7.3 mm Orthopedic surgical instrument component,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pega Medical Inc.
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Babi.Plus 12.5 cm H2O Pressure Relief Manifold Catalog # 2691 for use with ventilators.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Teleflex-Morrisville
FDA (openFDA device enforcement)
Reported Nov 6, 2019
A&E Medical Thorecon Plating System Kits Model No. 94-1200-08. For fracture fixation or reconstruction of the sternum.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alto Development Corp.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 6, 2019
AVKARE Ranitidine Hydrochloride Capsules 150 mg 500 Capsules Rx Only NDC 42291-735-50 UPC 342291735507 Manufactured…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AVKARE Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Nov 6, 2019
BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Nov 6, 2019
Cordis MAXI LD PTA Dilatation Catheter, for cardiovascular use.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Nov 6, 2019
CardioLab/ComboLab Recording Systems
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Nov 6, 2019
SPROTTE Lumbar with Introducer, labeled as the following: 1. Sprotte 22G x 90mm w/ introducer and wings (25/box); 2.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pajunk GmbH
FDA (openFDA device enforcement)
Reported Nov 6, 2019
POM Procedural Oxygen Masks, Endoscopic, Conscious Sedation, Bronchoscopy Mask, as follows: (1) POM Medical, LLC, REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.POM Medical LLC
FDA (openFDA device enforcement)
Reported Nov 6, 2019
Glam Day Nougat Candy packaged in 6-ounce (170g) plastic packages containing individually wrapped units identified only…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Rong Shing Trading NY Inc.
FDA (openFDA food enforcement)
Reported Nov 6, 2019
Synchro2, 0.014 in x 200cm, SOFT Guidewire with Hydrophilic Coating, UPN Product No. M00326010 REF 2601, STERILE: EO -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
7 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 6, 2019
Posey Connected Twice-As-Tough Cuffs
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tidi Products
FDA (openFDA device enforcement)
Reported Oct 30, 2019
Sterile Co-Flex NL 3" - Product Usage: Single Use secondary wound dressing or compression wrap.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Andover Healthcare Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 30, 2019
EXACTAMIX Empty EVA (Ethylene Vinyl Acetate) TPN Bag with the following product code and sizes: 1. H938737, 250mL; 2.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Oct 30, 2019
BD Vacutainer¿ Push Button Blood Collection Set with Pre-Attached Holder Catalog number 368356 - Product Usage: This…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Oct 30, 2019
ApexPro Telemetry Server System. Also identified as Modification To: ApexPro Telemetry System and ApexPro FH Telemetry…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Oct 30, 2019
The ICS CHARTR EP 200
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GN Otometrics
FDA (openFDA device enforcement)
Reported Oct 30, 2019
Irrisept Wound Debridement and Cleansing System. 12 units per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.IrriMAX Corporation
FDA (openFDA device enforcement)
Reported Oct 30, 2019
Premo and Fresh Grab Chicken Salad wheat sandwiches, 5 oz., with UPC code 612510002032.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lipari Foods Operating Company, LLC.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 30, 2019
Semi-Rigid Suction Canister, 3000cc. Model Numbers OR530 and OR530H. For OR530, the product comes in a case with two…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
FDA (openFDA device enforcement)
Reported Oct 30, 2019
Roland Brand Black Caviar - Whole Grain Lumpfish (Lumpfish Roe) packed in glass jars - 2oz & 2x2oz, UPC: 41224200029;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Roland Foods, LLC
1 more product in this recall
FDA (openFDA food 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.