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 Mar 12, 2014
Synthes 5.0mm Variable Locking Screw This device is part of the Variable Angle Locking Compression Plate family and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes, Inc.
FDA (openFDA device enforcement)
Reported Mar 5, 2014
Gelnique (oxybutynin chloride) Gel 10%, 100 mg in 1 g sachet, for topical use only. Physician sample in clamshell…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Actavis
FDA (openFDA drug enforcement)
Reported Mar 5, 2014
CSI, Diamondback 360 Coronary Orbital Atherectomy System, Part Number 70058-02, Model Number DBEC-125 Product Usage:…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cardiovascular Systems, Inc.
FDA (openFDA device enforcement)
Reported Mar 5, 2014
DMLC IV-ERGO Product Usage: Intended for use with rotating gantry linear accelerators to conform radiation dose…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Mar 5, 2014
GE Healthcare - Giraffe Warmer;Panda Warmer;Panda iRes Warmer, Giraffe Stand-alone Infant Resuscitation System. Product…
High riskUsing this product could cause serious injury, illness or death — stop using it now.GE Healthcare, LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 5, 2014
The FOCUS is a microprocessor controlled intra-oral x-ray unit with a Load Matching Frequency (LMF) DC generator, which…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumentarium Dental, PaloDEx Group Oy
FDA (openFDA device enforcement)
Reported Mar 5, 2014
Marlyce's Homemade Style Noodles, Net Wt. 8 oz, Packaged in plastic bags, 10 per case, UPC 094219217069. Manufactured…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.L. M. Noodle Company, LLC
FDA (openFDA food enforcement)
Reported Mar 5, 2014
ANGIOGRAPHY PACK; REF: DYNJ26855D; Packaged in Mexico by: Medline Industries, Inc., Mundelein, IL 60060; 1-800-Medline;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medline Industries, Inc.
10 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 5, 2014
Natural Grocers brand Dark Chocolate Almonds; six-ounce bags bearing UPC code 0-0008265007-0
High riskUsing this product could cause serious injury, illness or death — stop using it now.Natural Grocers by Vitamin Cottage
FDA (openFDA food enforcement)
Reported Mar 5, 2014
VITROS Chemistry Products Na+ Slides, manufactured by Ortho Clinical Diagnostics 513 Technology Blvd Rochester, NY…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 5, 2014
Single and Dual use Emission Computer Tomography gamma cameras (BrightView XCT, BrightView X & BrightView SPECT)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Mar 5, 2014
HeartStart MRx Monitor/Defibrillator; Model(s), Catalogue, or Code Number: M3535A, M3536A, M3536J, M3536MC The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 5, 2014
pCO2 D788 Membranes. Distributed by Radiometer America, Inc., Westlake, OH. An automatic or semi-automatic instrument…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Mar 5, 2014
Renasys EZ, a Canister Component of of Renasys EZ Negative Pressure Wound Therapy System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 5, 2014
PREMIER CARE RECLINER 5570 with Urethane armrests, Multiple side-table options, 3 position lock-bar, Fully upholstered,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Winco Mfg., LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 26, 2014
California Firm Recalls Canadian Liver P,tE Products Produced Without Import Inspection
High riskUsing this product could cause serious injury, illness or death — stop using it now.California Firm
USDA FSIS
Reported Feb 26, 2014
BACA'S GC Hot 12-13oz Z, Product Item Number 1010-0. Packaged in plastic containers. All packed in cardboard shipper…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.El Encanto, Incorporated
38 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 26, 2014
Synergy XVI XVI can incorrectly calculate the target position of the treatment table, because of an error that does not…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 26, 2014
GE Healthcare, PET Discovery 610, Discovery 710, Discovery 600 and Discovery 690. The GE Discovery XR and XA Systems…
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 Feb 26, 2014
Merit Medical's Custom Procedural Trays or Kits containing 1% Lidocaine HCl Injection, USP, 10 mg/mL, Lot 25-090-DK.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Merit Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Feb 26, 2014
Dried Tapioca Pearl, Net Wt. 7oz, 50 bags/carton, UPC Code 0893467803068
Moderate riskThis product could cause temporary or reversible health problems — stop using it.New Japan International, Inc.
FDA (openFDA food enforcement)
Reported Feb 26, 2014
Digestive enzyme capsules sold under the NOW Foods, Beeyoutiful, Best in Nature, Bluegrass Naturals Vitamin Company,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NOW Foods
FDA (openFDA food enforcement)
Reported Feb 19, 2014
5 x 93 US Probe Cover CMS-6049, Sterile, Single Patient Use. Custom Medical Specialties, Inc., Pine Level, NC, Federal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Custom Medical Specialties, Inc.
FDA (openFDA device enforcement)
Reported Feb 19, 2014
Malibu Polyaxial Screwdriver, 8.0 Plus, Model Number 91-2109; Malibu Polyaxial Screwdriver, Standard, Model Number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences 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.