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 48,100 notices were distributed nationwide, so they reach Virginia too — those are in the archive.
Reported Jul 14, 2021
FilmArray Pneumonia Panel (Pneumo) Part Numbers: Part No: RFIT-ASY-0144 / UDI: 00815381020178 (30 test kit) Part No:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 14, 2021
Verigene Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) Model Number: 20-006-024
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 14, 2021
CoreValve Evolut R Delivery Catheter System, REF: ENVEOR-L; ENVEOR-N;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Heart Valves Division
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 14, 2021
Yakult Nonfat Probiotic Drink; Live and active Lactobacillus casei Shitota; 2.7 FL. OZ. (80 mL), 5 individual bottles…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Yakult U.S.A. Inc.
FDA (openFDA food enforcement)
Reported Jul 7, 2021
5Fr PowerPICC Catheter Single-Lumen with 70cm Guidewire Instructions For Use: PowerPicc Polyurethand Radiology PiCC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Access Systems Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 7, 2021
Edwards TruWave (3 cc)/VAMP Jr 48 in (120 cm) Kit, REF: PXVJ356, Pressure Monitoring Set, RX Only, CE, Sterile EO,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
7 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 7, 2021
Tempus Pro - Patient physiological monitor, arrhythmia detector and alarm. Part No. - 00-1004-R, 00-1007-R, 00-1024-R,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remote Diagnostic Technologies Ltd.
FDA (openFDA device enforcement)
Reported Jul 7, 2021
Synaptive Trackable Suction Set Standard and Malleable
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synaptive Medical Inc.
FDA (openFDA device enforcement)
Reported Jul 7, 2021
Somerdale Red Dragon Cheddar Cheese, cut and repacked in plastic cheese wrap by Wegmans and sold by the pound.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wegmans Food Markets, Inc.
FDA (openFDA food enforcement)
Reported Jun 30, 2021
a.) Banner Smoked Fish Inc. brand Sliced Smoked Scotch Style Salmon (Salmon, Salt, Sugar, Natural Wood Smoke, Sodium…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Banner Smoked Fish Inc.
35 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 30, 2021
Access SARS CoV-2 lgG II Reagent, REF: C69057, IVD CE UDI: (01)15099590742744
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 30, 2021
inLight Medical LED Pads used with Polychromatic light technology system
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Inlightened Partners LLC
FDA (openFDA device enforcement)
Reported Jun 30, 2021
Medical Action INDUSTRIES INC., Disposable Instrument Pack Mosquito Hemostat, REF 56220
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Action Industries, Inc. 306
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 30, 2021
Philips Allura Xper System: Interventional Fluoroscopic X-Ray System Product No.: 722026, 722027, 722028, 722029,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems Nederlands
FDA (openFDA device enforcement)
Reported Jun 30, 2021
GENOSYL DS; Nitric Oxide Delivery System Combination Product NDA202860
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vero Biotech, LLC
FDA (openFDA device enforcement)
Reported Jun 23, 2021
Electrostatic Filter Angled, Item Code 350S19006 - Product Usage: indicated for single use on anesthetized patients and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien, LP
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 23, 2021
GE Healthcare Innova IGS 3 (GTIN 00840682147378), Innova IGS 5 (GTIN 00840682124621), Innova IGS 6 (GTIN…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Jun 23, 2021
BulkFoods.com brand dehydrated chopped celery in 1lb and 5lb plastic bags
High riskUsing this product could cause serious injury, illness or death — stop using it now.Natural Foods Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 23, 2021
OSSUR MIAMI J SELECT COLLAR - Product Usage: is intended to provide gross immobilization to the cervical spine. REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur Americas
FDA (openFDA device enforcement)
Reported Jun 23, 2021
Radiometer ABL90 FLEX Analyzer with E3800 PC units. The E3800 CPU is also used as spare part.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 16, 2021
DeRoyal Pacemaker Tray Pgybk, REF 89-6360.06
High riskUsing this product could cause serious injury, illness or death — stop using it now.DeRoyal Industries Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 16, 2021
Ruffles All Dressed Potato Chips 16 1/8 oz. packaged in flexible plastic bags UPC 28400 56520
High riskUsing this product could cause serious injury, illness or death — stop using it now.Frito-Lay, Inc. Headquarters
FDA (openFDA food enforcement)
Reported Jun 16, 2021
COVID-19 Self-Test Kit *** INNOVA *** 7T
High riskUsing this product could cause serious injury, illness or death — stop using it now.Innova Medical Group, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 16, 2021
Normand Remisol Advance Data Manager is a software device that interfaces between laboratory information systems (LIS)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Normand-Info S.A.S.U.
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.