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 48,124 notices were distributed nationwide, so they reach Virginia too — those are in the archive.
Reported Mar 11, 2015
DynaLOC Breast Interventional Planning Software Versions 3.1 and 3.2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.iCAD, Inc.
FDA (openFDA device enforcement)
Reported Mar 11, 2015
Ikaria, INOmax DSIR (Delivery System), Model 10007. Nitric oxide delivery system for use with ventilators.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.INO Therapeutics (dba Ikaria)
FDA (openFDA device enforcement)
Reported Mar 11, 2015
Izzio Artisan Bakery Rev Lem/Poppy Muffins 3.5oz packaged individually and put into cardboard case with 90 muffins per…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Izzio Artisan Bakery, LLC
FDA (openFDA food enforcement)
Reported Mar 11, 2015
GROUND CUMIN SEED, 50 LBS NET, ETO STERILE TREATED
High riskUsing this product could cause serious injury, illness or death — stop using it now.Morris J. Golombeck, Inc.
FDA (openFDA food enforcement)
Reported Mar 4, 2015
Starburst MRI Semi-Flex Electrode Device, 25cm/Attached Cable/14Ga/6.4F, Product No. H7877001039091, Catalog No.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics
FDA (openFDA device enforcement)
Reported Mar 4, 2015
Set Screw 5.5 mm Rod - Model #7703-1600. Product Usage: The titanium alloy set screw is used to seat a 5.5 mm titanium…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet Spine, LLC
FDA (openFDA device enforcement)
Reported Mar 4, 2015
The Centricity PACS Workstation is intended for use as a primary diagnostic and analysis tool for diagnostic images by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
FDA (openFDA device enforcement)
Reported Mar 4, 2015
HeartWare Ventricular Assist System (HeartWare Controller) Product Usage: For use as a bridge-to-cardiac…
High riskUsing this product could cause serious injury, illness or death — stop using it now.HeartWare Inc.
FDA (openFDA device enforcement)
Reported Mar 4, 2015
The Plum A+ Infusion System is designed to meet the fluid delivery requirements of today's evolving healthcare…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hospira Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 4, 2015
TDX Electric Wheelchair. Invacare FDX, TDX series and Storm Series (3G) power wheelchairs in 20 to 24 inch width…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 4, 2015
Philips Multi Diagnost Eleva II
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 4, 2015
CoCr Femoral Head - A modular head component is used in conjunction with a femoral stem component for replacement of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer GmbH
4 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 25, 2015
Mallory Head 4 Finned Acetabular Shell 50 mm, PN 13-104150, hip prosthesis component (Ringloc)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 25, 2015
Cold Therapy Pad - cold water circulating pad, one unit per package. The pads are used to provide a patient with local…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cincinnati Sub-Zero Products Inc.
FDA (openFDA device enforcement)
Reported Feb 25, 2015
BodyGuard 323 pump, models 100-510PXSI, 100-516PXS, 100-517PXS, 100-518PXS, 100-603XSA and 100-603XSAP
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CME America, LLC
FDA (openFDA device enforcement)
Reported Feb 25, 2015
Condies Foods, Bold & Zesty Salsa, 14 oz, UPC: 05077744220
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Condies Foods, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 25, 2015
Restoris Partial Knee Application (PKA) RIO (TGS 2.0). For use with the Robotic Arm Interactive Orthopedic System…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Feb 25, 2015
PROBAR Frosted Peanut Butter BASE Protein Bar, 2.46 oz film wrapped bar packaged in 12 wrapped units per sleeve/carton.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Probar LLC
FDA (openFDA food enforcement)
Reported Feb 18, 2015
Timberline Cranial Caudal and Posterior Blades, 40 - 180mm Model # 8734-2XXX, 8734-5XXX is a reusable device provided…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet Spine, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 18, 2015
The MAYFIELD¿ Ultra 360 Base Unit for head positioner, one unit per package. Product Usage: This product provides the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corporation
FDA (openFDA device enforcement)
Reported Feb 18, 2015
MorningStar Farms Spicy Black Bean Burger: 9.50 oz (4 ct) - UPC 2898939207; 18.90 oz (8 ct): UPC 2898971750; 8.7 lb…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kellogg USA Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Feb 18, 2015
Ground Cumin Seeds, ETO Treated, 50 lbs packaged in 50 lb brown paper bags
High riskUsing this product could cause serious injury, illness or death — stop using it now.Schiff Foods Products
FDA (openFDA food enforcement)
Reported Feb 18, 2015
MEDPOR Surgical Implant Contoured Two Piece Chin 5 mm; Part Number 86001; Lot Numbers A1405048, A1404026 Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Craniomaxillofacial Division
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 18, 2015
System 6 Aseptic Housing. The Stryker System 6 Aseptic Housings provide a sterile enclosure for the Stryker Non-sterile…
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)
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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.