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.

2,092 stored notices name West Virginia, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach West Virginia too — those are in the archive.

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)

Food

Reported Jun 28, 2017

PRIVATE SELECTION AFRICAN - INSPIRED PERI PERI CHILI CULINARY SPICE PASTE NET WT 4 OZ (113g) UPC 0 11110 80699 4…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Monfitello

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 28, 2017

Venture RX Catheter, Model 5820; Venture OTW Catheter, Model 5821; Venture CS Catheter, Model 5822. Sterilized using…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Vascular Solutions, Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 21, 2017

Spinach Sold under the brand names of Harris Teeter Farmers Market, 10 oz bag, PROUDLY DISTRIBUTED BY: HARRIS TEETER,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

The Horton Fruit Co. Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 14, 2017

Hudson RCI, Pediatric Nasal Cannula, Non-Flared Prongs, Rx only,

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Teleflex Medical

FDA (openFDA device enforcement)

Meat & poultry

Reported Jun 9, 2017

CC Kitchens, LLC Retira Productos De Ensalada De Carne Y Aves Debido A Posible Contaminación Con Listeria

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Recalling firm not stated

USDA FSIS

Medical devices

Reported Jun 7, 2017

Cardinal, Digital Bariatric Scale 1) model 6876, Cap 600 and 2) model 6868 Cap 1000

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cardinal Scale Mfg Co.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 7, 2017

NMT Patient Cable (989803174581) in use with lntelliVue NMT Module (Part# 865383)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Electronics North America Corporation

FDA (openFDA device enforcement)

Meat & poultry

Reported Jun 2, 2017

P&S Bakery, Inc. Recalls Pepperoni Product Due to Possible Foreign Matter Contamination

High riskUsing this product could cause serious injury, illness or death — stop using it now.

P&S Bakery, Inc.

USDA FSIS

Medical devices

Reported May 24, 2017

SoftPort Easy-Load Lens Delivery System Model: EZ-28V Is used for the folding and delivering of the LI61AO, LI61AOV, or…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bausch & Lomb Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 24, 2017

ETEST ETP32 (Ertapenem) Ref. 531640, 531600, blister packaging ETEST is a quantitative technique for determining the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

BioMerieux SA

FDA (openFDA device enforcement)

Medical devices

Reported May 24, 2017

enGen (TM) Laboratory Automation Systems using all TCAutomation(TM) Software Versions with the InOut Communication…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ortho-Clinical Diagnostics

FDA (openFDA device enforcement)

Free recall alerts

Get alerted about new West Virginia recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

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.