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 Apr 12, 2017
BrightView SPECT model number 882480 BrightView and BrightView X are gamma cameras designed for single or dual detector…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 5, 2017
AGFA Digital Radiography X-Ray System DX-D100 DX-D100 is indicated for use in providing diagnostic quality images to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AGFA Healthcare Corp.
FDA (openFDA device enforcement)
Reported Apr 5, 2017
JResultNet drivers using ASTM coding language. Calculator/data processing module, for clinical use - Stand-alone…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Data Innovations, LLC
FDA (openFDA device enforcement)
Reported Apr 5, 2017
Copper wood Colby Jack Mini Horn, 4/6#
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lipari Foods, Inc.
13 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 5, 2017
Buffalo Blue Kettle Cooked Potato Chips 8 oz (227g)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pinnacle Foods
FDA (openFDA food enforcement)
Reported Mar 29, 2017
Mammotome Revolve Dual Vacuum Assist Biopsy System The device is used to sample breast tissue that has been identified…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Devicor Medical Products Inc.
FDA (openFDA device enforcement)
Reported Mar 29, 2017
AMS-636, 60" Microbore extension set. Product Usage: Accessory devices used to administer medical fluids.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vygon MFG, Inc., dba/ Churchill Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Mar 22, 2017
Terumo Advanced Perfusion System 1-Level Sensor II Pads, Product Usage: Ultrasonic couplant used to facilitate the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 22, 2017
Toshiba Kalare DREX-KL80 X-ray generator
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Toshiba American Medical Systems Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 15, 2017
Great Shake Fortified Nutrition, Soy Formula, Chocolate Artificially Flavored, Packaged in 4 fl oz. (118 mL), and 6 fl…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hormel Foods Corporation
5 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 15, 2017
Private Selection, Salted Caramel Chocolate Almond Pie, NET WT 34 OZ ( 2 LB 2 OZ) 963g, UPC 1111054021. Container: In a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Legendary Baking
FDA (openFDA food enforcement)
Reported Mar 15, 2017
Remel, Haemophilus Test Medium (Agar) in A) 100 mm REF R01503, and B) 150 mm plates REF R04033,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Inc.
FDA (openFDA device enforcement)
Reported Mar 8, 2017
BD AffirM VPIII Microbial Identification Test
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Mar 8, 2017
Check-Flo Performer Introducer, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 8, 2017
EliA Sample Diluent, Article number, 83-1023-01
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Phadia US Inc.
FDA (openFDA device enforcement)
Reported Mar 1, 2017
ETEST XM256 (Cefuroxime), Foam: 506958-506918; SPB: 412304-412305 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)
Reported Mar 1, 2017
Tosoh Bioscience HLC-723G8 Analyzer for HbA1c testing.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tosoh Bioscience, Inc.
FDA (openFDA device enforcement)
Reported Mar 1, 2017
Keyspan High-High Speed USB to Serial Adapter Product Usage: The Reporting Software is an application which serves as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tosoh Smd Inc.
FDA (openFDA device enforcement)
Reported Feb 28, 2017
Wayne Farms, LLC Recalls Ready-To-Eat Chicken Products Due To Potential Processing Deviation
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wayne Farms LLC
USDA FSIS
Reported Feb 24, 2017
Fsis Issues Public Health Alert for Meat and Poultry Wraps Due to Possible Listeria Contamination
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.JLM Manufacturing
USDA FSIS
Reported Feb 22, 2017
Discovery MR450 The systems are whole body magnetic resonance scanners designed to support high resolution, high…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Feb 22, 2017
Stryker Restoris RIO Reamer Handle, Offset, Mako Rx only Product Usage: The handle is used to hold surgical components…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Feb 22, 2017
LIFEPAK 15 Monitor, Automated External Defibrillator (AED), Manual mode monitoring and therapy functions are intended…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Physio-Control, Inc.
FDA (openFDA device enforcement)
Reported Feb 22, 2017
CentraLink¿ Data Management System Software Versions: v13x,v14x,v15x The CentraLink system software is a network…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
2 more products in this recall
FDA (openFDA device 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.