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 Jul 10, 2019
Draco Enzymatic Deep-Cleaning Pad with Ready-to-Use Enzymatic Detergent, Product Number HY0305Z
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Madison Polymeric Engineering
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 10, 2019
Sorghum, Mfg. by Ozark Country Sorghum, Dunnegan, MO 65640, Net Wt. 2 lb. 14 OZ. packaged in glass jars
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ozark Country Kitchen
FDA (openFDA food enforcement)
Reported Jul 10, 2019
Vereos PET/CT, Model No. 882446 Product Usage: Positron Emission Tomography (PET) and X-ray Computed Tomography (CT)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jul 10, 2019
WOODSTOCK ORGANIC GRILLED RED PEPPER, NET WT 10. OZ, packaged in a plastic packaged marked with UPC Code: 4256301714.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.UNFI General Corporate
FDA (openFDA food enforcement)
Reported Jul 10, 2019
DVR Crosslock ePAK Screw Driver, Model Number 212000002 Product Usage: These DVR Express Disposable Instruments are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 3, 2019
Plain Cheesecake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hank's Cheesecakes, LLC
22 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 26, 2019
Aquarius D13S319 Plus Deletion Probe, Model LPH068-A Product Usage: The D13S319 probe, labelled in red, covers a 156kb…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cytocell Ltd.
FDA (openFDA device enforcement)
Reported Jun 26, 2019
2.7 Degree Angled Sagittal Saw attachment (Mako Total Knee Application Only)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 26, 2019
Cepheid Xpert C. difficile/Epi Control Panel
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Microbiologics Inc.
FDA (openFDA device enforcement)
Reported Jun 19, 2019
IntraClude Intra-Aortic Occlusion Device, REF: ICF100, 10.5 Fr (3.5 mm) X 39.4" (100 cm), Rx Only, Sterile EO The…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported Jun 19, 2019
Prestige II, Prestige SI, Prestige VH Prestige system is a new multi-purpose conventional and digital R/F remote…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 19, 2019
xTAG Gastrointestinal Pathogen Panel intended for the simultaneous qualitative detection and identification of multiple…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Molecular Diagnostics
FDA (openFDA device enforcement)
Reported Jun 19, 2019
Terumo Advanced Perfusion System 1 Electronic Patient Gas System (EPGS), Electronic Gas Blender, Catalog #: 801188, UDI…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
FDA (openFDA device enforcement)
Reported Jun 12, 2019
Alinity c Cuvette Segments, List Number 04S47-01 Product Usage: The Alinity c Cuvettes are used on the Alinity c system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott GmbH & Co. KG
FDA (openFDA device enforcement)
Reported Jun 12, 2019
MRSASelect, IVD, REF 63747, containing 20 plates per package. The MRSASelect is indicated for use in conjunction with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2019
Regimen 28 Day - Glutaraldehyde Sterilizing and Disinfecting Solution
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kerr/Pentron, dba Kerr Corporation and Pentron Clinical
FDA (openFDA device enforcement)
Reported Jun 12, 2019
Leica Cryostats, used to produce frozen sample sections for biological, medical and industrial applications, including…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Jun 12, 2019
Cepheid Xpert MRSA/MRSA NxG Control Panel (Catalog #8195) UDI: 70845357041226 Product Usage: On April 9, 2019,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microbiologics Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2019
ECMO Reinforced Dual Lumen Cannula, Sterile EO, Rx Only, REF: VV16F
High riskUsing this product could cause serious injury, illness or death — stop using it now.OriGen Biomedical, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2019
Stryker Neurovascular, AXS Infinity LS Plus Long Sheath, Rx Only, Sterile EO, USA Customer Service 855-91 NEURO…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
FDA (openFDA device enforcement)
Reported Jun 5, 2019
Abbott MitraClip XTR Clip Delivery System, UDI: 08717648226366, Part: CDS0601-XTR, Sterile EO, Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Vascular
FDA (openFDA device enforcement)
Reported Jun 5, 2019
Horizon Cardiology Hemo
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Change Healthcare Israel Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 5, 2019
Dole Classic Coleslaw (US) Shredded cabbage and carrots. 14 oz. US
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dole Fresh Vegetables
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 5, 2019
Colby Jack Cheese in 40 pound and 640 pound blocks
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hilmar Cheese Company, Inc.
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.