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.
2,087 stored notices name West Virginia, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach West Virginia too — those are in the archive.
Reported May 20, 2026
Edwards EVOQUE tricuspid delivery system REF:9850TDS Sterile EO
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported May 13, 2026
ERBEFLO CleverCap CO2: Hybrid CO2 Tubing/Cap Set for Olympus Scopes & CO2 Sources, REF: 20325-239; Hybrid CO2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Erbe Medical, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 13, 2026
french broad CHOCOLATE bette's bake sale (a multi-flavor bonbon assortment). 6-piece NET WT. 2.5 OZ (70.75G); 12-piece…
High riskUsing this product could cause serious injury, illness or death — stop using it now.French Broad Chocolate Factory
FDA (openFDA food enforcement)
Reported May 13, 2026
Intuitive 8 mm SureForm 30 Gray Reloads Reference Numbers: 48230M-05 and 48230M-06
High riskUsing this product could cause serious injury, illness or death — stop using it now.Intuitive Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 13, 2026
LIFEPAK 15, REF: 99577-000025, 99577-000047, 99577-001256, 99577-001217, 99577-001241, 99577-001255, 99577-001219,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
FDA (openFDA device enforcement)
Reported May 6, 2026
Brand Name: HiResolution" Bionic Ear System Product Name: M Zn-Air Battery Pak Model/Catalog Number: CI-5501-110;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Bionics, LLC
FDA (openFDA device enforcement)
Reported May 6, 2026
Brand Name: Kiwi Omni Vacuum Delivery System Product Name: Kiwi Omni Vacuum Delivery System Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Clinical Innovations, LLC
FDA (openFDA device enforcement)
Reported May 6, 2026
Brand Name: Leksell Vantage Arc System REF: 1053958
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Apr 22, 2026
Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp. (NeuroSciences)
4 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 22, 2026
Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wilson-Cook Medical Inc.
FDA (openFDA device enforcement)
Reported Apr 15, 2026
Vital Nutrients Aller-C (vitamin C, citrus bioflavonoids, isoquercitrin, and bromelain)100 count bottles and 200 count…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Blueroot Health, Inc.
FDA (openFDA food enforcement)
Reported Apr 8, 2026
" Dumpling Vegetable 4.5 oz 011110658067 " Loaded Dumpling Vegetable 5.7 oz 011110696953
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Jfe Franchising Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 8, 2026
MiniMed 670G Insulin Pump (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed, Inc.
13 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 8, 2026
Jiffy Original Composite Polisher Cups (Coarse) 12pk, REF 7011.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ultradent Products, Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2026
BD Alaris" System with Guardrails" Suite MX with Point of Care Unit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2026
Volar Radius Plate with Angular Stability with the following description: Radius Plate PROlock II. Article Numbers:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.I.T.S. GmbH
16 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2026
MiniMed" 780G - MMT-1884 MiniMed" 780G - MMT-1886 With Software 6.60 and 6.61
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed, Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2026
CentrosFLO Hemodialysis Catheters, REF: CENFP15K/A, CENFP15K/B, CENFP17K/A, CENFP19K/A, CENFP23K/A, CENFP27K/A,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Merit Medical Systems, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 25, 2026
Brand Name: Leksell Gamma Knife Product Description: Leksell Gamma Knife¿ Perfexion Leksell Gamma Knife¿ Icon" Leksell…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Mar 25, 2026
Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100 TABLETS UPC 3 15826 16910 2;…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Winder Laboratories, LLC
FDA (openFDA food enforcement)
Reported Mar 18, 2026
PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog Numbers: 11101-000016 UDI-DI code:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
FDA (openFDA device enforcement)
Reported Mar 11, 2026
Gelsoft Plus, REF: 635024PE, 631514PE, 631222PE, 633008PE, 633010PE, 633007PE, 636010PE, 632522PE, 633012PE, 635018PE,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vascutek, Ltd.
FDA (openFDA device enforcement)
Reported Feb 25, 2026
MONARCH Platform, Bronchoscopy, Catalog Numbers: MON-000005-01 , MON-000005-01R , MON-000006 , MON-000006-RFB,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Auris Health, Inc.
FDA (openFDA device enforcement)
Reported Feb 25, 2026
Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff Cat 60060
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
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.