All recall categories

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.

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Food

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Food

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Food

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Food

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)

Medical devices

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)

Medical devices

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)

Food

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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Other states

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.