Recalls distributed in Virginia
These notices name 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.
4,732 stored notices name Virginia, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,132 notices were distributed nationwide, so they reach Virginia too — those are in the archive.
Reported Aug 14, 2013
Cordis OPTEASE Retrieval Inferior Vena Cava (IVC) Filter***REF Cat. No.***466F220A and 466F220B***Vena Cava Filter and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cordis Corporation
FDA (openFDA device enforcement)
Reported Aug 14, 2013
Sunny Sea Sardines in Tomato Sauce, 24 cans/case, 15 oz.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Golden Beach Inc.
FDA (openFDA food enforcement)
Reported Aug 14, 2013
MRidium 1145 Dose Reduction System (DERS) drug library kit. (This is an option for the MRidium 3860+MR Infusion Pump…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Iradimed Corporation
FDA (openFDA device enforcement)
Reported Aug 14, 2013
Nestle Nutrition, Compat, Enteral Feeding Tube, sterile, 8 French (REF 08310400), 10 French (REF 08310600), and 12…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nestle HealthCare Nutrition
FDA (openFDA device enforcement)
Reported Aug 14, 2013
Earth's Pride Organics: Organic Oregano, 2.2 oz. Packaged at 12 units per case. Packaged in a glass jar with cork…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Olde Thompson, Inc.
FDA (openFDA food enforcement)
Reported Aug 14, 2013
TCM4 series Base Units, and spare part Power Supply, Radiometer Medical ApS, Akandevej 21, Br¿nsh¿j, Denmark,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Aug 14, 2013
Dimension Tacrolimus Flex reagent cartridge (DF107) and Dimension TACR CAL (DC107) Product Usage: The TACR method is an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2013
Sonopet Ultrasonic Aspirator Console (Console 110V with Pedal & Pole) Product Usage: The Sonopet Console is indicated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2013
Raw Pistachio Halves, 1 pound bag. Item Number 11910, UPC Code: 172043119107; Raw Pistachio Halves, 4 pound bag. Item…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Superior Nut Co. Inc.
FDA (openFDA food enforcement)
Reported Aug 7, 2013
Custom Spine ISSYS LP Inverted Screw System. 8.5MM X 45 MM ISSYS LP Screw Rx Non-Sterile. Custom Spine, Inc. 9 Campus…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Custom Spine, Inc.
FDA (openFDA device enforcement)
Reported Aug 7, 2013
LPS Lower Extremity Dovetail Intercalary component. Intended for use in replacement of the mid-shaft portion of the…
High riskUsing this product could cause serious injury, illness or death — stop using it now.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Aug 7, 2013
GE Healthcare, VOLUSON E6, E8, E8 EXPERT, E10 DIAGNOSTIC ULTRASOUND SYSTEM. The device is a general purpose ultrasound…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 7, 2013
Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HeartWare Inc.
FDA (openFDA device enforcement)
Reported Aug 7, 2013
WHOLEY Shrimp, Farm Raised, Cooked, Peeled Deveined, Tail on, Ingredients: Shrimp, Salt and Sodium Tripolyphosphate...,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lipari Foods, Inc.
FDA (openFDA food enforcement)
Reported Aug 7, 2013
OSKRI, Coconut Bar Dark Chocolate, Net Wt. 1.9 oz ( 53g), UPC 6 66016 30070 3. Ingredients: Coconuts 55%, Rice Syrup,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Oskri Corp.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 7, 2013
AIA Analyzer Pipette Tips used on Tosoh AIA-2000, AIA-1800, AIA-900 and AIA-600II Analyzers, 1000 tips/bag AIA-Analyzer…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tosoh Smd Inc.
FDA (openFDA device enforcement)
Reported Aug 7, 2013
Pimento Cheese, packaged in 7 oz. plastic containers, and labeled in part ***Made by Whole Foods Market, Landover, MD…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Whole Foods Market Mid-Atlantic Kitchen
FDA (openFDA food enforcement)
Reported Jul 31, 2013
Advanced Orthogonal Percussion Adjusting Instrument Indicated for use by a licensed Chiropractor to assist in making…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Orthogonal Equipment, Incorporated
FDA (openFDA device enforcement)
Reported Jul 31, 2013
Endopath Electrosurgery Probe Plus II, twelve (12) different devices, including hooks, spatulas, right angles, curved…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 31, 2013
HemosIL RecombiPlasTin 2G, Part Number 0020002950 (8 ml size). The product is used for the evaluation of the extrinsic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumentation Laboratory Co.
FDA (openFDA device enforcement)
Reported Jul 31, 2013
Magnesium Sulfate 2 grams in Dextrose 5% for Injection, in 50 mL Plastic Infusion Bags, Med Prep Consulting Inc.,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Med Prep Consulting, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jul 31, 2013
Dermalight 80 Model Number UVB-080, one unit per box. The Dermalight 80 is a Phototherapy light unit that provides…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.National Biological Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 31, 2013
Rultract Retractor Ratchet Cover Plate Distributed by Pemco, Inc., Cleveland, OH 44131 Surgical retractor used to lift…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pemco Inc.
FDA (openFDA device enforcement)
Reported Jul 31, 2013
STERIS Fine Traction Device, one unit per box Product Usage: The Fine Traction Device is used to provide traction and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Virginia recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.