All recall categories

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.

Medical devices

Reported Dec 22, 2021

Miami J Select Collar, Item: MJS-101, and Miami J Select Collar Set, Item: MJSR-101 Instructions for Use

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ossur Americas

FDA (openFDA device enforcement)

Food

Reported Dec 22, 2021

The Mustard Man Inc Simply Peppered Mustard 8oz plastic bottles, 6 bottles per case

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

The Mustard Man Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 15, 2021

SuperCore Biopsy Instrument: REF/Product Description: 701114090/SUPERCORE BIOPSY INSTR 14GA X 9CM; 701114150/SUPERCORE…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Argon Medical Devices, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 8, 2021

BioFire Blood Culture Identification 2 (BCID2) Panel Part No: RFIT-ASY-0147 UDI: 00815381020338 Blood Culture Catalog…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Food

Reported Dec 8, 2021

Tastykake Buttercreme Iced Creme Filled Chocolate Cupcakes 14.25oz (6-2ct) box UPC 0 25600 00230 8 & 2.375oz package,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Flowers Foods (Corporate Offices)

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 8, 2021

GE Centricity Universal Viewer Zero Footprint Client

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 8, 2021

The Steripath Gen2 Blood Collection System Model Number/Description 2700-21-EN / Steripath Gen2 Blood Collection System…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Magnolia Medical Technologies, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 8, 2021

NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System: Model Number/Item Number/Product…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

NuVasive Specialized Orthopedics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 8, 2021

RANDOX CHOL-cholesterol (total) test system intended to measure cholesterol in plasma and serum REF: CH200

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Randox Laboratories Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 1, 2021

ARCHITECT i1000SR REF 01L86-01/1L86 and 1L87; ARCHITECT i2000SR REF 03M74-02/3M74; ARCHITECT i2000 REF 08C89-01/1G17…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Laboratories

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 1, 2021

Endurant Stent Graft System REF/Description: ENTF2525C70EE STENT GRAFT ENTF2525C70EE ENDURANT TUBE

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Vascular, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 1, 2021

Garden Side Salad 6.95oz. (197g) UPC:72251525202. Packaged in plastic containers.

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Ukrop's Homestyle Foods, LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 24, 2021

BIO-RAD BioPlex 2200 REF 12000650 SYPH T PACK Syphilis Total & RPR Reagent Pack The BioPlex Syphilis Total & RPR kit is…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bio-Rad Laboratories, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 24, 2021

Vit Kit-Freeze is intended for use in assisted reproductive procedures for vitrification and storage of human oocytes…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Fujifilm Irvine Scientific, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 24, 2021

VITROS Immunodiagnostic Products Anti-HBc IgM Controls, Product Code 6801427 For use in monitoring the performance of…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Ortho-Clinical Diagnostics, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 17, 2021

Country Oven Cinnamon Roll 4oz, 2.5oz

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

The Kroger Co.

18 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 10, 2021

FIVE S 3.5x65, Flexible Intubation Videoscope, REF: 091361-01 (1 Unit), and 091361-06 (6 Units)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Karl Storz Endoscopy

FDA (openFDA device enforcement)

Medical devices

Reported Nov 10, 2021

IPL Coupling Gel, I L (AX1009013), 12 pack of 0.25 L (AX1009018), 6 pack of 1 L (AX1009019 or AX1009063); and IPL…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Lumenis, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 3, 2021

ASC PneumoLiner device, Part No. WA90500US (US market only) The Pneumoliner device is intended for use as a multiple…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Olympus Corporation of the Americas

FDA (openFDA device enforcement)

Food

Reported Nov 3, 2021

Simply Nature Organic Poppy Seed Dressing

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Schlotterbeck & Foss LLC

FDA (openFDA food enforcement)

Food

Reported Nov 3, 2021

Almond Flour Crackers fine ground sea salt packaged in a white box with yellow graphics weighing 4.25 oz. Label reads…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Simple Mills

FDA (openFDA food enforcement)

Medical devices

Reported Nov 3, 2021

REF/Catalogue Number GSX0030A, GORE CARDIOFORM SEPTAL OCCLUDER 30 mm Diameter, Catheter Working Length 75 cm, Delivery…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

W L Gore & Associates, Inc.

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 27, 2021

SIMPLEXA COVID-19 Positive Control Pack, REF MOL4160, IVD, Rx Only, UDI: (01) 20816101027051

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

DiaSorin Molecular LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 27, 2021

VITROS Immunodiagnostic Products Anti-SARS-CoV-2 IgG Quantitative Controls (IVD)- For use in monitoring the performance…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ortho Clinical Diagnostics Inc.

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.