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 May 18, 2022
1) ACS Spine Pack 2) ACS Lumbar/Back Set Up Tray
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Contract Systems, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported May 18, 2022
putty i-FACTOR Peptide Enhanced Bone Graft 1.0cc Syringe REF 700-010, PUTTY
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cerapedics, Inc.
FDA (openFDA device enforcement)
Reported May 18, 2022
The following first aid kits and cabinets containing components Medi-First XS Non-Aspirin, Product #80450, 2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Certified Safety Mfg Inc.
FDA (openFDA device enforcement)
Reported May 18, 2022
1 Series CX phototherapy units equipped with Daavlin's ClearLink Control System software versions v3.03h and 3.04v.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Daavlin Distributing Company
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 18, 2022
Bwell Bird's Nest Beverage Pandan Flavor NET 8.45 FL OZ (250mL) UPC 8373726342 24 bottles per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eastland Food Corporation
5 more products in this recall
FDA (openFDA food enforcement)
Reported May 18, 2022
HemosIL ReadiPlasTin, Part No. 0020301400
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumentation Laboratory
FDA (openFDA device enforcement)
Reported May 18, 2022
11001RD1 11001RDK1 KARL STORZ Slim Nasopharyngolaryngoscope 96216006US V5.0 (10-2018)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
11 more products in this recall
FDA (openFDA device enforcement)
Reported May 18, 2022
Medtronic IN.PACT Admiral, Paclitaxel-coated PTA Balloon Catheter, Sterile EO, Rx Only for the following model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Vascular, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 18, 2022
ProterixBio SARS-CoV-2 (RBD) IgG Antibody Test, and associated ProterixBio Dried Blood Spot Collection Kit, no model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Proterixbio
FDA (openFDA device enforcement)
Reported May 18, 2022
OnGuard2 CSTD Bag Adaptor SP A Chemfort CSTD Product, Product code MG412143
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Simplivia Healthcare Ltd.
FDA (openFDA device enforcement)
Reported May 18, 2022
Diagnostic Kit SARS-cCo V Antigen Rapid Test
Moderate riskThis product could cause temporary or reversible health problems — stop using it.USA Medical, LLC
FDA (openFDA device enforcement)
Reported May 11, 2022
Olive; TOP SAVOR Licorice Flavored Olive; Net wt: 500g (17.63oz); Ingredients: olive, sugar, salt, licorice extract,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.A & C Best Food Trading
2 more products in this recall
FDA (openFDA food enforcement)
Reported May 11, 2022
K-Wire, 1.35 mm x 170 mm
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported May 11, 2022
TRAY RING COVER, REF OM271000, CONTAINS (1) TRAY RING COVER, STERILE R, Rx Only,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Johnson & Johnson Surgical Vision Inc.
FDA (openFDA device enforcement)
Reported May 11, 2022
Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold); COVID 19 Test
High riskUsing this product could cause serious injury, illness or death — stop using it now.SML Distribution, LLC
FDA (openFDA device enforcement)
Reported May 4, 2022
ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carl Zeiss Meditec AG
FDA (openFDA device enforcement)
Reported May 4, 2022
da Vinici X da Vinci Xi Sureform 45 REF 480445 da Vinci X da Vinci Xi Sureform 45 Curved-Tip REF 480545 da Vinici X da…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported May 4, 2022
MEDTRONIC INTERSTIM THERAPY SYSTEM FOR URINARY CONTROL, which includes the following: a) Handset with Communicator,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported May 4, 2022
NeuMoDx Cartridge-For in vitro diagnostic use with NeuMoOx Molecular Systems with either of the following assays:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NeuMoDx Molecular Inc.
FDA (openFDA device enforcement)
Reported May 4, 2022
Rebel Pistachio Ice Cream, one pint (473 mL, UPC 8 53149 00821 1, Manufactured by Rebel Creamery LLC, Midway, UT 84049.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rebel Creamery
FDA (openFDA food enforcement)
Reported May 4, 2022
Convenience kits containing regard IV Start Kits: (1) regard Clinical Packaging Solutions, Item Number: 830014015,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ROi CPS LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 4, 2022
syngo.via RT Image Suite upgraded to VB60 running on syngo.via Model Number 10496180. Running on servers with syngo.via…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 4, 2022
TearCare version 1.0 SmartHubs
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sight Sciences, Inc.
FDA (openFDA device enforcement)
Reported May 4, 2022
Organic Marketside Zucchini 2 Count packages/8 per case Ingredients: Organic Zucchini New WT. 6 oz. (170g) UPC:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.World Variety Produce Inc. dba Melissa's
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.