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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.

Medical devices

Reported Aug 26, 2015

Siemens Symbia S Series system, a diagnostic analog or digital detector based planar (2- dimensional) nuclear medicine…

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

Siemens Medical Solutions USA, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 26, 2015

Stryker Orthopaedics Triathlon X3 Tibial Bearing Insert - CR REF 5530-G-209 (component of the Triathlon Total Knee…

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

Stryker Howmedica Osteonics Corp.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 26, 2015

Bronchial Double Lumen Tube Set (Left), Sterile

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

Teleflex, Inc.

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 12, 2015

Merge Hemo, 9.10, 9.20.0, 9.20.1,9.20.2, 9.30, 9.40.0, 9.40.1, 9.40.2 with Massimo PHASEIN End Tidal CO2 (EtCO2)…

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

Merge Healthcare, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 12, 2015

18inch Dual Port/Single Bladder Disposable Tourniquet Cuff, Zimmer Surgical, Inc. Tourniquets are intended to be used…

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)

Food

Reported Aug 5, 2015

Fat Free Pasteurized Prepared Cheese Product: SOUTHHOME 12/12OZ AMERICAN FAT FREE YELLOW, 0788001319. ROUNDYS 12/12OZ…

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

Dairy Farmers OF America Inc.

33 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 5, 2015

Paragon Laboratory Management

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

McKesson Technologies, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 5, 2015

Invivo Expression MRI Patient Monitoring System.

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

Philips Electronics North America Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 5, 2015

Computed Tomography X-ray Systems Brilliance CT 64-channel with Essence technology. Intended to produce cross-sectional…

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

Philips Medical Systems (Cleveland) Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2015

Bausch & Lomb SofPort Advanced Optics Aspheric Lens

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

Bausch & Lomb Surgical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2015

Ring Transjugular Intrahepatic Access Set Product Usage: The Ring Transjugular Intrahepatic Access Sets are intended…

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

Cook Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2015

ATTUNE FB PS ARTICULATION SURFACE SIZES 3-8 INTENDED USE: The Tibial Articulation Surface Trial snaps together with the…

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

DePuy Orthopaedics, Inc.

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2015

ADVIA Centaur Tni-Ultra Assay; SMN 10317708 - 100 tests and SMN 10317709 -500 tests Product Usage: For in vitro…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2015

0702-001-350Q, Diverter Valve Assembly 0702-001-000, Neptune 2 Rover Ultra (120V) 0702-001-000R, Repair Neptune 2 Rover…

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

Stryker Instruments Div.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2015

Various OxyTOTE Portable Oxygen System regulators, Valve Integrated Pressure Regulator, one unit per package. Product…

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

Western / Scott Fetzer Company

FDA (openFDA device enforcement)

Medical devices

Reported Jul 22, 2015

MOSAIQ Oncology Information System MOSAIQ is an oncology information system used to manage workflows for treatment…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 22, 2015

Allofix Insertion Kit, 2.0 mm, Single Drill, Product Usage: MTF Surgical Instruments are designed for the specific…

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

Musculoskeletal Transplant Foundation, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 15, 2015

DASANI Purified Water, 24/20 fl. oz. (1.25 pt) 591 mL, pack, Desani, The Coca Cola Company, Atlanta, GA 30313.

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

World

FDA (openFDA food enforcement)

Medical devices

Reported Jul 8, 2015

Etest Cefotaxime CT 256 WW and Etest Cefotaxime CT 256 US. in vitro diagnostic.

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

BioMerieux SA

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2015

Velocity" Biopsy Valve, 25 units per box, Product Usage: The disposable Velocity biopsy valve is used to cover the…

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

US Endoscopy Group Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 1, 2015

Raw Macadamia Nuts, packaged in 8 oz. plastic cup, packaged under the Aurora and private labels as follows:Belmont…

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

Aurora Products, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 1, 2015

LapSac Surgical Tissue Pouch. The current intended use for the LapSac Surgical Tissue Pouch is for isolating tissue…

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

Cook Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 1, 2015

Deskins Candies, Chocolate No Bakes, Net Wt. 16-oz., packaged in 1 lb. plastic containers containing 8-10 cookies / 12…

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

Deskins Wholesale, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jun 24, 2015

Amerigel Hydrogel Gauze Dressing 2 x 2, A5002. Wound Management.

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

Amerx Health Care Corp.

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.