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.
Reported Feb 27, 2019
AMIA Automated Peritoneal Dialysis System Product Usage: It is intended for automatic control of dialysate solution…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 27, 2019
Randox CALCIUM (Ca) Colorimetric Method RX Series Cat. No. CA 3871, R1. Arsenazo Reagent 9 x 51ml GTIN: 05055273200904
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 20, 2019
MOSAIQ¿ Oncology Information System and Sequencer MOSAIQ is an oncology information system used to manage workflows for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Feb 13, 2019
ARCHITECT Free T3 Reagent Kit used on ARCHITECT i1000SR or i2000/i2000SR platforms Product Usage: It is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Ireland Diagnostics Division
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 13, 2019
Henry Schein CU 1000 Halogen Curing Light, Catalog 900-4542. - Product Usage: Curing light for use in dentistry. The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Handpiece Headquarters
FDA (openFDA device enforcement)
Reported Feb 13, 2019
Clancy's Wavy Potato Chips, 10 oz., UPC 0 41498 16306 8
High riskUsing this product could cause serious injury, illness or death — stop using it now.Olde York Potato Chips
FDA (openFDA food enforcement)
Reported Feb 13, 2019
Product: ABL800 FLEX with Crea. The ABL800 with Crea is available in the following configurations: ABL817, ABL827 and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Feb 6, 2019
Peaches, sold as a bulk retail item, with PLU 4044, and country of origin of Chile. The peaches sold at Aldi are…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Jac Vandenberg Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 6, 2019
Calix Lumbar Spinal Implant System: 22mm x 10mm x 7mm PLIF ASSY PC, REF X034-0172PC 22mm x 10mm x 8mm PLIF ASSY PC, REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Xtant Medical Inc.
FDA (openFDA device enforcement)
Reported Jan 30, 2019
Perfusion Pack, Rx only, Sterile EO
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA
FDA (openFDA device enforcement)
Reported Jan 28, 2019
Perdue Foods, LLC Recalls Refrigerated Fun Shapes Chicken Breast Nuggets Due to Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.Perdue Foods, Llc.
USDA FSIS
Reported Jan 23, 2019
Arthrex Suture Anchor, Nano Corkscrew FT (consists of an anchor pre-loaded on a handled inserter including suture, with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported Jan 16, 2019
Various GE Magnetic Resonance System on-site software version Product Usage: Magnetic resonance imaging equipment for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 9, 2019
StealthStation Cranial and Synergy Cranial Depth Gauge: StealthStation Cranial Optical Pocket Guide - Instructions for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Jan 9, 2019
Enamelast Cool Mint/OT Varnish 5% NaF Mint Label Enamelast Unit Dose 200pk Cool Mint: Enamelast 5% Sodium Fluoride Unit…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ultradent Products, Inc.
FDA (openFDA device enforcement)
Reported Jan 2, 2019
GEM Coupler Forceps, GEM4183C, packaged individually.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Jan 2, 2019
HydroSet XT Injectable HA Bone Cement, REF 897003, STERILE
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 2, 2019
Thermoset Room Temperature Closed Loop Injectate Delivery System. 1 unit per Cavity #3 Cavity Deep/20 pieces per case…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 2, 2019
Medtronic MiniMed 630G 6025805-003_C, Rx Only Medtronic MiniMed 670G 6025805-005_B, Rx Only Medtronic MiniMed 640G…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc.
FDA (openFDA device enforcement)
Reported Jan 2, 2019
SP CAL (LIQ), REF IT2692 This product is intended for in vitro diagnostic use with Randox Alpha-1-Antitrypsin,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories Ltd.
FDA (openFDA device enforcement)
Reported Jan 2, 2019
ROOT 23 CUCUMBER HABANERO SIMPLE SYRUP 375 ml
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Root 23 LLC
FDA (openFDA food enforcement)
Reported Dec 26, 2018
Wegmans Roasted Corn and Bean Salad; 13 oz. Plastic Container, 40 oz. Plastic Container, 4.5 lb. Plastic Bulk Container
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ASK Foods Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 26, 2018
enVista One Piece Hydrophobic Acrylic Intraocular lens - Is indicated for primary implantation for the visual…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bausch & Lomb Surgical, Inc.
FDA (openFDA device enforcement)
Reported Dec 26, 2018
VITEK 2 Antimicrobial Susceptibility Testing (AST) using one or more of these susceptibility products: Catalog #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.bioMerieux, Inc.
1 more product in this recall
FDA (openFDA device 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.