Recalls distributed in West Virginia
These notices name West Virginia 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.
2,055 stored notices name West Virginia, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach West Virginia too — those are in the archive.
Reported Sep 6, 2017
iVue with Normative Database, Device Listing Number D185549. Product Usage: The iVue (K121739) is a non-contact, high…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Optovue, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 6, 2017
Toshiba America Medical Systems Ultimax Digital Fluoroscopic X-Ray System Model: DREX-UI80 Ultimax is intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Toshiba American Medical Systems Inc.
FDA (openFDA device enforcement)
Reported Aug 30, 2017
DBS Lead Depth Stop contained in Medtronic Deep Brain Stimulation (DBS) lead kits, models 3387/3387S, 3389/3389S, and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Aug 30, 2017
Tissu-Trans Filtron 100, 3-TT-FILTRON 100. Product Usage: Intended for fat transfer and liposuction.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shippert Medical Technologies
6 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 30, 2017
Taylor Farms Creamy Homestyle Coleslaw Kit, dressing included. Green Cabbage, Carrots, Red Cabbage and Creamy coleslaw…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Taylor Farms Retail, Inc.
FDA (openFDA food enforcement)
Reported Aug 23, 2017
Arctic Sun 5000 Temperature Management System, 100-120 V North America and 100-120 V US
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Aug 23, 2017
VNS Therapy¿ AspireHC¿ Generator, VNS Therapy¿ AspireSR¿ Generator. Model No. 105. Product Usage: United States…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cyberonics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 9, 2017
InflammaDry(R) AN RPS DIAGNOSTIC SOLUTION, Sample Collectors InflammaDry(R) is a rapid, immunoassay test for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quidel Corporation
FDA (openFDA device enforcement)
Reported Aug 9, 2017
Spectranetics Turbo-Elite Laser Atherectomy Catheter Peripheral Rapid Exchange Catheters Device is indicated for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spectranetics Corporation
FDA (openFDA device enforcement)
Reported Aug 2, 2017
STOCKERT Heater-Cooler System 3T, 230 V
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sorin Group USA, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 26, 2017
Agfa Healthcare NX 3.0.8950 Imaging Processing Software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AGFA Healthcare Corp.
FDA (openFDA device enforcement)
Reported Jul 26, 2017
Futaba Sesame Hijiki Rice Seasoning; 2.29 oz. glass jar; 4 902533 023173
High riskUsing this product could cause serious injury, illness or death — stop using it now.J F C International Inc.
FDA (openFDA food enforcement)
Reported Jul 26, 2017
Penumbra 3D Revascularization Device It is indicated for used in the revascularization of patients with acute ischemic…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Penumbra Inc.
FDA (openFDA device enforcement)
Reported Jul 26, 2017
Artis zee,x-ray system, angiographic Artis zee is a family of dedicated angiography systems developed for single and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Jul 19, 2017
Beckman Coulter Synchron AQUA CAL Level 1, Part No. 471288 Product Usage: Used for the system calibration of Na, K, Cl,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Jul 19, 2017
Simple truth Dry Roasted Macadamia Nuts 12 oz bags UPC 0 1111 00247 8 DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kroger Corporate Food Technology Laboratory
FDA (openFDA food enforcement)
Reported Jul 19, 2017
The Olympic Pasteurmatic 3000 and Olympic Pasteurmatic 3500 are intended for cleaning and high-level disinfection of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Medical Incorporated
FDA (openFDA device enforcement)
Reported Jul 19, 2017
Nicolet¿ Elite¿ 2 MHz OB Probe, Non-Fetal Monitor, Model #: X1L007, Catalog Code: N200. Intended for non-invasive…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Neurology Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 19, 2017
ATAR Reusable Extension Cable, sold under brand names: ATAR Reusable Series, ATAR 53912 Reusable Series, and XI…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Oscor, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 19, 2017
Video Duodenoscope These instruments are intended to provide optical visualization of (via a video monitor), and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pentax
FDA (openFDA device enforcement)
Reported Jul 12, 2017
Giant Eagle; Toasted Crumb Tilapia; various weights; Dist. By: Giant Eagle, Inc., Pittsburgh, PA PLU #69123. UPC:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Giant Eagle, Inc.
FDA (openFDA food enforcement)
Reported Jul 12, 2017
Nussloch GmbH ASP6025 Tissue Processor
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Jul 12, 2017
Electrophysiology catheter cables are designed as electrode cables with a multi-pin connector on the distal end and the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sterilmed Inc.
FDA (openFDA device enforcement)
Reported Jul 5, 2017
Kroger Dessert Cups yellow sponge cakes NET WT 6.5 oz (184g) INGREDIENTS: ***NONFAT M ILK***CONTAINS: WHEAT, EGGS, SOY.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Kroger Co.
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.