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 27, 2014
Magna-Fx Cannulated Screw Fixation System Bone Screw Fully Threaded Sterile zimmer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
15 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 20, 2014
DX-D 600 - DXD Imaging Package Product Usage:Is indicated for use in providing diagnostic quality images to aid the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AGFA Healthcare Corp.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 20, 2014
Allegro Original Marinade, 12.7 fl oz (375 mL), UPC 0 74964 00100 7
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Allegro Fine Foods Inc.
FDA (openFDA food enforcement)
Reported Aug 20, 2014
BD Multi Check CD4 Low Control Catalog No. 340916 is intended as a complete process control for immunophenotyping by…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.BD Biosciences, Systems & Reagents
FDA (openFDA device enforcement)
Reported Aug 20, 2014
VIDAS D-Dimer Exclusion II, an automated quantitative test for use on instruments of the VIDAS family for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported Aug 20, 2014
Device Brand Name: Distal Radius Fracture Repair System Device Classification Name: Plate, Fixation, Bone Device Common…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
FDA (openFDA device enforcement)
Reported Aug 20, 2014
Esaote PA230E Transducer A portable and cart base ultrasound system for general and cardiovascular imaging
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biosound Esaote, Inc.
FDA (openFDA device enforcement)
Reported Aug 20, 2014
Codman Certas - In Line Valve Only; Product Code: 82-8800 The Codman Certas Programmable valve is an implantable device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Codman & Shurtleff, Inc.
7 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 20, 2014
Frederick Farms 4oz chocolate ice cream cups, net wt. 67grams, 24 per box, 231 boxes per pallet, expiration 6-10-15
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Garber Ice Cream Company Inc.
FDA (openFDA food enforcement)
Reported Aug 20, 2014
Medical Positioning Rapid Response HUT table, Powered Medical Examination table, Model # 1017. Product Usage: Used to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Positioning Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 20, 2014
Medtronic Ascenda Intrathecal Catheter models 8780 and 8781, and Ascenda Intrathecal Catheter Pump Segment Revision…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Aug 13, 2014
AdvanDx Quick FISH Fixation Kit for BC ( Blood Cultures), 50 tests. In vitro diagnostic. The QuickFISH Fixation Kits…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advandx Inc.
FDA (openFDA device enforcement)
Reported Aug 13, 2014
Alcohol-Free Hand Sanitizer, 1. fl. oz. (30 ml) bottles capped with white sprayer, OTC, contains Benzalkonium chloride.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HLI dba Humphreyline Inc.
FDA (openFDA drug enforcement)
Reported Aug 13, 2014
Sonopet Ultrasonic Surgical System Console, Ultrasonic Aspirator, Stryker Medtech.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Aug 6, 2014
Patient Data Manager 2.0 (Content manager 2.0, Patient Browser 4.0, DICOM Viewer 2.0) Brainlab Digital Lightbox. A…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Aug 6, 2014
Horizon Medical Imaging It is a medical image and information management application that is intended to receive,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson Medical Immaging
FDA (openFDA device enforcement)
Reported Aug 6, 2014
Medtronic Nexdrive Micropositioning Drive. Models Ml-1000 and Ml-2000. For use in conjunction with the Medtronic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Aug 6, 2014
Henry Schein Natural Elegance SE Bond Self-Etch Light-Cure Adhesive contains 50 0.125 mL unit dose tips, 50 applicator…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Novocol, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 6, 2014
InTouch Critical Care Bed, Stryker Medical. Model Numbers 2130, 2131, 2140, 2141, 2151, 2152, 2155, and 2156.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
FDA (openFDA device enforcement)
Reported Aug 6, 2014
IPM Wound Gel Rx Wound Dressing IPM Wound Gel is indicated for the management of wound healing.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wellspring Pharmaceutical Corporation
FDA (openFDA device enforcement)
Reported Jul 30, 2014
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)
Reported Jul 30, 2014
PRAN brand Spice Powder TURMERIC, Net Wt. 8.82 oz./250g, UPC 8 31730 00551 --- PRODUCT OF BANGLADESH -- Manufactured…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Asia Cash & Carry Inc.
FDA (openFDA food enforcement)
Reported Jul 30, 2014
RECLAIM Taper Protector Sleeve. RECLAIM Revision Hip System Orthopedic Manual Surgical Instrument, used to ensure the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 30, 2014
MK5 NX Controller--Wheelchair controller
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
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.