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 Jul 10, 2013

Computed Tomography X-ray systems Product Usage: The Brilliance CT 64, Ingenuity Core, and Ingenuity Core128 scanners…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 3, 2013

Enzyme Solutions, A Dietary Supplement, Formula 29, 8 oz. (226.8g), UPC Code 697706041408. Distributed by: Enzyme…

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

Enzyme Formulations, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 3, 2013

DC power cable (p/n 3010556) supplied with the MEDRAD(R) Veris MR Vital Signs Monitor: Product Usage: Monitor,…

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

Medrad Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 3, 2013

Brilliance CT 64, Ingenuity CT, Ingenuity Core, and Ingenuity Core128 scanners are whole body Computed Tomography X-ray…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 26, 2013

GE Healthcare, PET VCAR. PET VCAR application software is affected if installed on any of the following versions of the…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jun 26, 2013

VITROS Chemistry Products-HCY Reagent packaged in a kit carton. Catalog# 6802002. Used to quantitatively measure total…

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

Ortho-Clinical Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Jun 26, 2013

GlideScope Video Laryngoscope (GVL) 3, 4, 5 and GlideScope (AVL) 2, 3, 4 and 5 reusable blades Product Usage: The…

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

Verathon, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 19, 2013

TX1 Tissue Removal System disposable handpieces. Product Usage: The TX1 Tissue Removal System is indicated for use in…

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

American Optisurgical Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 19, 2013

XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy Joint Function, 90 and…

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

Atlantic Pro Nutrients, Inc. dba XYMOGEN

FDA (openFDA food enforcement)

Food

Reported Jun 19, 2013

IGA Brand Vanilla & Chocolate Ice Cream, 1.75 Quart

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

Dairy Fresh LLC

FDA (openFDA food enforcement)

Food

Reported Jun 19, 2013

Chicken Noodle Soup Mix, "9 oz cello bag, Contents: All natural enriched semolina flour***PURELY AMERICAN 5991…

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

Purely American, Inc.

10 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 12, 2013

AGFA Digital Radiography X-Ray System DX-D 100 Agfa's DX-D 100 is indicated for use in providing diagnostic quality…

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

AGFA Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2013

FLEXSTENT Biliary Self-Expanding Stent System. Product Usage: The FSS FLEXSTENT Biliary SES product is indicated for…

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

Cordis Corporation

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2013

BrightView SPECT gamma camera for Emission Computed Tomography, Philips Medical Systems, Cleveland, OH 44143 BrightView…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2013

EZ Breathe Atomizer Model # EZ-100. For the delivery of liquid medications for respiratory usage.

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

Nephron Pharmaceuticals Corp.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2013

***REF S-3D*** 3mm Diamond Ball. Used for cutting and shaping bone.

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

The Anspach Effort, Inc.

FDA (openFDA device enforcement)

Drugs

Reported May 29, 2013

Rite Aid brand Maximum Strength Tussin Cough & Cold Mucus Relief CF, (dextromethorphan HBr 10 mg, guaifenesin 200 mg…

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

Aaron Industries Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported May 29, 2013

Cardinal Health hCG Cassette Rapid Test, Part Number: B1077-22 (Mfg PN: 4582105026) The SP hCG Cassette Rapid Test is a…

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

Alere San Diego, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 29, 2013

Brilliance CT 16-Slice Water, System Code: 728245; Brilliance CT 10-Slice Water, System Code: 728250; Brilliance CT…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 15, 2013

KARL STORZ Photodynamic Diagnosis (PDD) D-Light C System, Instruction Manuals: PDD Telescopes, Tricam SL II, and PDD…

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

Karl Storz Endoscopy America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 15, 2013

Olympus SurgMaster UES-40 electrosurgical unit ("UES-40") Product Usage: Designed for use in a medical facility under…

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

Olympus America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2013

STERRAD CYCLESURE 24 Biological Indicator (BI) The STERRAD CYCLESURE 24 Biological Indicator (BI), is intended to be…

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

Advanced Sterilization Products

FDA (openFDA device enforcement)

Medical devices

Reported May 8, 2013

Diacap(R) Ultra Dialysis Fluid Filter, Catalog Number 7107367. Intended to filter bacteria and endotoxins from dialysis…

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

B. Braun Medical, Inc.

FDA (openFDA device enforcement)

Food

Reported May 8, 2013

BUFFALO TRACE BOURBON FLAVORED CARAMEL SAUCE 8 oz glass jars Net Wt. 8 fl. oz./227 g, PRODUCED BY: APPLECREEK ORCHARDS…

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

Buffalo Trace Distillery

4 more products in this recall

FDA (openFDA food 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.