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.
2,088 stored notices name West Virginia, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,765 notices were distributed nationwide, so they reach West Virginia too — those are in the archive.
Reported Jun 15, 2022
Triathlon Tritanium Tibial Component (Size 6); Catalog Number 5536-B-600 Triathlon¿ Tritanium¿ Tibial Component (Size…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
FDA (openFDA device enforcement)
Reported Jun 15, 2022
STORZ KARL STORZ-ENDOSKOPE REF 11272VUE CMOS Video Cysto-Urethroscope REF 11272VUEK CMOS Video Cysto-Urethroscope…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
FDA (openFDA device enforcement)
Reported Jun 15, 2022
Pimlico Confectioners Vegan Fine Hazelnut Truffles in a 3.88-ounce green plastic package.
High riskUsing this product could cause serious injury, illness or death — stop using it now.The TJX Companies, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 8, 2022
In-Line ventilator adaptor
High riskUsing this product could cause serious injury, illness or death — stop using it now.Baxter Healthcare Corporation
7 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2022
BD Anti-Kappa APC (Cat. No. 341098) is an analyte specific reagent for the Anti-Kappa antibody, which specifically…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company, BD Biosciences
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2022
DYNEX Agility, Agility Analyzer, Model No. 67000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dynex Technologies, Inc.
FDA (openFDA device enforcement)
Reported Jun 8, 2022
The C304-HIS device features a guide wire to access the vein, a valve to reduce blood loss during the implant…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
FDA (openFDA device enforcement)
Reported Jun 8, 2022
JIF CREAMY PEANUT BUTTER packaged in 18gram, 500gram, 1 kilogram, 1.1oz (120 count)12oz, 16oz, 28oz, 40oz, 48oz, 4lb…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The JM Smucker Company LLC
23 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 8, 2022
Jason & Mary Large Milk Peanut Butter Cup
High riskUsing this product could cause serious injury, illness or death — stop using it now.Walnut Creek Chocolate Co. Inc.
14 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 1, 2022
HydroMARK Breast Biopsy Marker, Model No. 4010-05-08-T4
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Devicor Medical Products Inc.
FDA (openFDA device enforcement)
Reported Jun 1, 2022
Vanta INS Implantable Neurostimulator. Medtronic Model 977006 Vanta with AdaptiveStim Technology Neurostimulator with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 1, 2022
Mrs. Miller's Homemade Jam Smokey BBQ Bacon Jam packaged into 9 oz glass jar 12 jars per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mrs Millers Homemade Jams LLC.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 1, 2022
(1) Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile; (2) Gibeck Humid-Vent 2S Flex DC, Product #17732,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 25, 2022
VITRIGUARD, CARRIER, CLEAR; Model. No. 43782001 The VitriGuard device is a cryopreservation storage device composed of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported May 25, 2022
Getinge 9100-Series Washer Disinfector models: 9120E, 9125E, 9127E, 9128E, 9122EW, 9128EW.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge USA Sales Inc.
FDA (openFDA device enforcement)
Reported May 25, 2022
CK MB Calibrator, Catalogue Number CK2393
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Randox Laboratories Ltd.
FDA (openFDA device enforcement)
Reported May 18, 2022
The following first aid kits and cabinets containing components Medi-First XS Non-Aspirin, Product #80450, 2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Certified Safety Mfg Inc.
FDA (openFDA device enforcement)
Reported May 18, 2022
1 Series CX phototherapy units equipped with Daavlin's ClearLink Control System software versions v3.03h and 3.04v.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Daavlin Distributing Company
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 18, 2022
Bwell Bird's Nest Beverage Pandan Flavor NET 8.45 FL OZ (250mL) UPC 8373726342 24 bottles per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eastland Food Corporation
5 more products in this recall
FDA (openFDA food enforcement)
Reported May 18, 2022
HemosIL ReadiPlasTin, Part No. 0020301400
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumentation Laboratory
FDA (openFDA device enforcement)
Reported May 18, 2022
Medtronic IN.PACT Admiral, Paclitaxel-coated PTA Balloon Catheter, Sterile EO, Rx Only for the following model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Vascular, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 18, 2022
OnGuard2 CSTD Bag Adaptor SP A Chemfort CSTD Product, Product code MG412143
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Simplivia Healthcare Ltd.
FDA (openFDA device enforcement)
Reported May 13, 2022
FSIS Issues Public Health Alert for Weis Markets’ Ready-To-Eat General Tso Chicken Meals Due to Misbranding and…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Fsis
USDA FSIS
Reported May 4, 2022
ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carl Zeiss Meditec AG
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.