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 28, 2018
Pentax Video Duodenoscope Model: ED-3490TK (UDI of design being recalled: 04961333232420) These instruments are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pentax
FDA (openFDA device enforcement)
Reported Feb 21, 2018
Lyophilized Chemistry Calibrator Level 1 Product Usage: Beckman Coulter Chemistry Calibrators are intended for use when…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Feb 21, 2018
WALNUT CREEK FOODS Caramel Popcorn NET WT 15 OZ (425g) Ingredients: Evaporated Can Juice, Popcorn, Butter (cream,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Coblentz Distributing Inc. dba Walnut Creek Foods
FDA (openFDA food enforcement)
Reported Feb 21, 2018
Carestation 620 A1, Carestation 650 A1, and Carestation 650c A1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems China Co., Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 21, 2018
A.T.S. 4000TS Tourniquet Systems, Personalized Pressure. Intended to be used by qualified professionals to temporarily…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Surgical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 14, 2018
ACE(TM) BRAND, ULTRA LITE ANKLE brace: (a) Size Selection Medium, Cat #901014, UPC 051131019984 2; (b) Size Selection…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.3M Company - Health Care Business
FDA (openFDA device enforcement)
Reported Feb 14, 2018
AIRO Mobile CT System, Model Number: MobiCT-32 Product Usage: The AIRO is intended to be used for X-ray computed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Feb 14, 2018
DRILL BIT MINI QUICK CONNECT 1.0MM, REF 2312-20-200 & 2312-20-202, NON STERILE
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 7, 2018
Clover Valley¿ Iced Oatmeal Cookies NET WT 12 OZ (340 g) CONTAINS: WHEAT, SOY. DISTRIBUTED BY DOLGENCORP, LLC 100…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dollar General Corporation, Inc.
FDA (openFDA food enforcement)
Reported Feb 7, 2018
Elements Obturation Unit (EOU) used with respective Buchanan Heat Pluggers Device is an endodontic root canal plugger.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ormco/Sybronendo
FDA (openFDA device enforcement)
Reported Jan 24, 2018
ACCOLADE SR Pacemaker
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
23 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 24, 2018
Frozen Tuna Fillet Saku (Restaurant Supply Only); 22 lbs./2 x 5 kgs. Wild caught: Handline with Hook. Keep Frozen - 18…
High riskUsing this product could cause serious injury, illness or death — stop using it now.H.I.G. Corporation
FDA (openFDA food enforcement)
Reported Jan 24, 2018
Unifine Pentips 5mm x 31G pen needles, packaged in 100 ct pen needles. Product Usage: Sterile, non-toxic,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Owen Mumford USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 17, 2018
Cordis S.M.A.R.T. Flex Biliary Stent System Product Usage: Is indicated for use in the palliation of malignant…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Jan 17, 2018
UNIVERSAL FLEX2 BREATHING CIRCUIT, Item Numbers: D460-6133Z, D390-6121Z, D390-6121Z, D495-61Z, DF4116-6121Z, D466-61Z,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.King Systems Corp. dba Ambu, Inc.
FDA (openFDA device enforcement)
Reported Jan 17, 2018
SHS Wel-Plan Wheat and Corn Strach Baking Mix , 400 g box,Cardboard carton, 18 cartons per case, but distributed by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nutricia North America
FDA (openFDA food enforcement)
Reported Dec 27, 2017
Xper Flex Cardio Physiomonitoring system. Used to facilitate invasive investigations of heart and vascular disease when…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invivo Corporation
FDA (openFDA device enforcement)
Reported Dec 20, 2017
Dark Chocolate Almonds packaged under the brand names: (1)Wegmans, 23 OZ (1 LB 7 OZ) 652g tub UPC: 0 77890 328200 4 and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.First Source, LLC
6 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 20, 2017
Dark Chocolate Coffee Beans, Natural Dark Chocolate Coffee Beans
Moderate riskThis product could cause temporary or reversible health problems — stop using it.JLM Manufacturing LLC
4 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 20, 2017
ABL800 analyzer with FLEXQ module. Device intended for in vitro testing of samples of whole blood for the parameters…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Dec 13, 2017
Fit & Active Chocolatey Chip Protein Meal Bars; UPC: 41498 18695; Lot Code: Q209MY; Expiration date: May 24, 2018
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leclerc Foods USA
FDA (openFDA food enforcement)
Reported Dec 13, 2017
89291 Cashew Tower (Plow and Hearth Chocolate Covered Cashews). Net weight: 10 ounces . The product is package as a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Plow And Hearth
FDA (openFDA food enforcement)
Reported Dec 13, 2017
Comforts FOR BABY Purified Water with Flouride Added. 1 GAL (3.78 L) DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Kroger Co.
FDA (openFDA food enforcement)
Reported Dec 6, 2017
Dark Chocolate Almond, Net 11 oz., Contains Almond and Soy, Distributed By: Dutch Valley Food Distributors, Inc.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dutch Valley Food Distributors Inc.
1 more product in this recall
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.