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 48,122 notices were distributed nationwide, so they reach Virginia too — those are in the archive.
Reported Sep 14, 2016
NOMAD Pro Packaged X-Ray System, Part Number 08500009; NOMAD Pro Vet Packaged X-Ray System, Part Number 08500011; NOMAD…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aribex Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 14, 2016
ArjoHuntleigh Sara Combilizer; Intended to facilitate early immobilization, rehabilitation, and care of patients.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ARJOHUNTLEIGH POLSKA Sp. z.o.o.
FDA (openFDA device enforcement)
Reported Sep 14, 2016
Hard Tissue Replacement (HTR) Implant, Rx only, for use in single procedure only. Custom made. HTR polymer implants are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet Microfixation, LLC
FDA (openFDA device enforcement)
Reported Sep 14, 2016
PF Chang's Home Menu Brand Shrimp Lo Mein, UPC 3100067005, 22 oz bag, 4 bags per case, ConAgra Foods, Omaha, NE 68102
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConAgra Frozen Foods, Inc.
FDA (openFDA food enforcement)
Reported Sep 14, 2016
Lysander's Premium Teriyaki Marinade, 1 oz (28 g), polypropylene and clamshell style card, 12 units per case.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Geneva Foods, LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 14, 2016
Inland Market, Premium Blue Crab Spread, Net Wt. 7 oz. (198 g.) and 16 oz. (454g), Inland Market, 1667 Lewis Way, Stone…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Inland Seafood, Inc.
10 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 14, 2016
Integra Cranial Access Kits, Catalogue Nos. INSHITH; INSHITHRZN; INSHITHND
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp. d.b.a. Integra Pain Management
FDA (openFDA device enforcement)
Reported Sep 14, 2016
The system provides the ability to transmit patient data files for storage, viewing and analysis at distributed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invivo Corporation
FDA (openFDA device enforcement)
Reported Sep 14, 2016
Methylprednisolone Acetate/Lidocaine HCl 40/10 mg/mL Injection, 10 mL multidose vial, sterile. Rx only. Compounded by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Isomeric Pharmacy Solution, LLC
FDA (openFDA drug enforcement)
Reported Sep 14, 2016
Sterile Drape, SK6000 PAQ drape pouch (for use with the SPY Fluorescent System (SPY 2000/2001)) The SPY Fluorescent…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Novadaq Technologies Inc.
FDA (openFDA device enforcement)
Reported Sep 14, 2016
Activia FIBER Lowfat Yogurt Strawberry/Pineapple Flavors 12 Packs of 4 OZ Cups UPC 3663202884 packaged in form fill…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Dannon Company, Inc.
FDA (openFDA food enforcement)
Reported Sep 7, 2016
Euro Custard Cake, Plastic wrapped cardboard container (Net Wt. 7.20 oz.)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Eastland Food Corporation
FDA (openFDA food enforcement)
Reported Sep 7, 2016
INTEGRA Spinal Tray, Catalogue No: 3404875, Contents: 10 Each per Case, Sterile.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp. d.b.a. Integra Pain Management
FDA (openFDA device enforcement)
Reported Sep 7, 2016
Chili Dog, Low Fat/Low Sodium Product ID 952000
High riskUsing this product could cause serious injury, illness or death — stop using it now.Let's Do Lunch, Inc.
8 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 7, 2016
Double Pump RF Patient Cassette; Product Number: 72204055. Intended to provide fluid distension and irrigation and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Vision Ab
FDA (openFDA device enforcement)
Reported Sep 7, 2016
A7 Anesthesia Delivery System, a device used to administer to a patient, continuously or intermittently, a general…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mindray DS USA, Inc. dba Mindray North America
FDA (openFDA device enforcement)
Reported Sep 7, 2016
SPECULAR MICROSCOPE CEM-530; Software version 1.08 and 1.09. Opthalmic: The NIDEK Specular Microscope CEM-530 provides…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nidek Inc.
FDA (openFDA device enforcement)
Reported Sep 7, 2016
Kale, 4/ 1 lb, & 1 /2 lb shredded packaged in plastic, keep refrigerated
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pearson Foods Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Aug 31, 2016
Adult ThermoGard¿ Dual Dispersive Electrodes (for patients >15 kg.), 10' (3.05m) Cable, Catalog Number 51-7310.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Conmed Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Large QWIX Compression screw, dia. 7.5 mm L 90 mm, Lot No. FH86, Rx only, Product Usage: The QWIX Positioning screw is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Aug 31, 2016
RadSuite software. The firm name on the label is Merge Healthcare, Hartland, WI.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Radiesse (+) Lidocaine, Injectable Implant 1.5cc, Rx only, P/N: 8063M0K1, Merz Aesthetics. Product Usage: RADIESSE is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merz North America, Inc.
FDA (openFDA device enforcement)
Reported Aug 31, 2016
TIGR Matrix Surgical Mesh, Model No. NSTM1015, NSTM1520, NSTM2030
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Novus Scientific Ab
FDA (openFDA device enforcement)
Reported Aug 31, 2016
Brilliance 64 CT Model number 728231 Product Usage: Computed Tomography X-ray systems intended to produce…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
6 more products in this recall
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.