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 Jun 24, 2026
iLet Bionic Pancreas, REF: BB1001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beta Bionics, Inc.
FDA (openFDA device enforcement)
Reported Jun 24, 2026
TRI TS BASEPLATE SIZE 3. Part Number: 5521-B-300.
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 Jun 24, 2026
Mito Red Light, Super Mobile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mito Red Light Inc.
FDA (openFDA device enforcement)
Reported Jun 24, 2026
Nutrisystem, Chocolate Cheesecake, 2 oz (57g) packages, Flow Wrapped, 48 units per case, Keep frozen
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nutrisystem Inc.
FDA (openFDA food enforcement)
Reported Jun 24, 2026
Product Name: STAAR ICL Calculation Software Software Version: Version 8.00 Product Description: The STAAR ICL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Staar Surgical AG
FDA (openFDA device enforcement)
Reported Jun 17, 2026
Merlin" Patient Care System (PCS) software Merlin" PCS 3650 programmer Model 3330 software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Medical
FDA (openFDA device enforcement)
Reported Jun 17, 2026
Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx30mm Model/Catalog Number: CND0830
Moderate riskThis product could cause temporary or reversible health problems — stop using it.INSPIREMD Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number: H938175 Product Description:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Jun 10, 2026
BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Becton Dickinson & Company
9 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Brand Name: Da Vinci 5 Product Name: ASSY,DV5 TOWER,IS5000 Model/Catalog Number: 380746 Software Version: N/A Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Jun 10, 2026
My Wife's Slaw, packaged in 8 oz. and 16 oz. glass mason jars with metal lids/bands, MyWifeslaw.web.app, Zanesville,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Jesse Withrow
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 10, 2026
Digital Angiography System Trinias:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST safire:UD150G-40 /…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Medical Systems
FDA (openFDA device enforcement)
Reported May 27, 2026
Swan-Ganz Catheter, Models: 131F7/131F7P, 131F7J, 141F7, 151F7, 834F75, 096F6/096F6P, C144F7, 782F75M, 132F5, C146F7,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 27, 2026
Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement, Net Wt. 8 FL Oz (237mL) Amber PET modern round 24-400…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Llorens Pharmaceuticals International Division, Inc.
FDA (openFDA food enforcement)
Reported May 20, 2026
Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM iOS App Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dexcom, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 20, 2026
Brand Name: DONJOY Product Name: ICEMAN CLASSIC CUBE Model/Catalog Number: 11-0494 Software Version: no Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Djo, LLC
3 more products in this recall
FDA (openFDA device enforcement)
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)
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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.