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 Dec 22, 2021
The Mustard Man Inc Simply Peppered Mustard 8oz plastic bottles, 6 bottles per case
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.The Mustard Man Inc.
FDA (openFDA food enforcement)
Reported Dec 15, 2021
SuperCore Biopsy Instrument: REF/Product Description: 701114090/SUPERCORE BIOPSY INSTR 14GA X 9CM; 701114150/SUPERCORE…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Argon Medical Devices, Inc.
FDA (openFDA device enforcement)
Reported Dec 15, 2021
GERBER Macaroni and Cheese with a side of peas and carrots, 6.6 oz. (187 g) drained weight 5.3 oz. (150 g), 8 units per…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Gerber Products Company dba Nestle Infant Nutrition
FDA (openFDA food enforcement)
Reported Dec 15, 2021
Mountain Meadow Herbs Brand Candida Flush Endotoxin Cleans3, 500 mg per capsule, 240 capsules per bottle. UPC 8 13086…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mountain Meadow Herbs, Inc.
FDA (openFDA food enforcement)
Reported Dec 15, 2021
O3D ORCHESTRATE Orthodontic Technologies User Manual and Data Processing Instructions (model preparation for tooth…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orchestrate Orthodontic Technologies, Inc.
FDA (openFDA device enforcement)
Reported Dec 15, 2021
OsteoMed OsteoPower Power Console: -OsteoMed OsteoPower Power Console 2 REF 450-0021-00 -OsteoMed D-Power Control…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Osteomed, LLC
FDA (openFDA device enforcement)
Reported Dec 15, 2021
Minute Maid Berry Punch, 59 Fl. oz. (1.8 QT) 1.75 L, Unit UPC: 025000047664; Case UPC: 025000047671
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Coca Cola Company
2 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 15, 2021
Trader Joe's Organic Blue Corn Tortilla Chips: 16 oz. bag, 15 bags per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trader Joes Company
FDA (openFDA food enforcement)
Reported Dec 8, 2021
BioFire Blood Culture Identification 2 (BCID2) Panel Part No: RFIT-ASY-0147 UDI: 00815381020338 Blood Culture Catalog…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported Dec 8, 2021
SHIP KIT, PROCEDURE KIT, PROTEKDUO LS - DL31 for temporary Cardiopulmonary bypass. Including the following components:…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cardiac Assist, Inc.
FDA (openFDA device enforcement)
Reported Dec 8, 2021
Tastykake Buttercreme Iced Creme Filled Chocolate Cupcakes 14.25oz (6-2ct) box UPC 0 25600 00230 8 & 2.375oz package,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Flowers Foods (Corporate Offices)
5 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 8, 2021
The Steripath Gen2 Blood Collection System Model Number/Description 2700-21-EN / Steripath Gen2 Blood Collection System…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Magnolia Medical Technologies, Inc.
FDA (openFDA device enforcement)
Reported Dec 8, 2021
"Herbal Doctor" brand Angelicae Sinensis, Natural Herb, Net Wt. 16 oz (454 g) packaged in a green plastic bag; and 12oz…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Murray International Trading Co., Inc.
FDA (openFDA food enforcement)
Reported Dec 8, 2021
NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System: Model Number/Item Number/Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NuVasive Specialized Orthopedics, Inc.
FDA (openFDA device enforcement)
Reported Dec 8, 2021
RANDOX CHOL-cholesterol (total) test system intended to measure cholesterol in plasma and serum REF: CH200
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories Ltd.
FDA (openFDA device enforcement)
Reported Dec 8, 2021
Abbott HeartMate Touch Communication System, REF: HMT1100 (US), HMT1100-R (Rental US), HMT1150 (EU)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec Corp.
FDA (openFDA device enforcement)
Reported Dec 1, 2021
ARCHITECT i1000SR REF 01L86-01/1L86 and 1L87; ARCHITECT i2000SR REF 03M74-02/3M74; ARCHITECT i2000 REF 08C89-01/1G17…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 1, 2021
BD Nexiva, 20 GA 1.00 IN (1.1 X 25 mm), 3660 ml/hr. 61ml/min; Closed IV Catheter System- Dual port -61 mL/min (3660…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson Infusion Therapy Systems Inc.
FDA (openFDA device enforcement)
Reported Dec 1, 2021
HemosIL ReadiPlasTin (20 mL), Part number 0020301400. An in vitro diagnostic thromboplastin reagent.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumentation Laboratory
FDA (openFDA device enforcement)
Reported Dec 1, 2021
Endurant Stent Graft System REF/Description: ENTF2525C70EE STENT GRAFT ENTF2525C70EE ENDURANT TUBE
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Vascular, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 1, 2021
Freelite Human Lambda Free Kit (for use on the SPAPLUS) REF LK018.S Freelite Human Lambda Free Kit (for use on the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Binding Site Group, Ltd.
FDA (openFDA device enforcement)
Reported Dec 1, 2021
Garden Side Salad 6.95oz. (197g) UPC:72251525202. Packaged in plastic containers.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Ukrop's Homestyle Foods, LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 24, 2021
BIO-RAD BioPlex 2200 REF 12000650 SYPH T PACK Syphilis Total & RPR Reagent Pack The BioPlex Syphilis Total & RPR kit is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 24, 2021
Dole Garden Salad; iceberg lettuce, shredded carrots, red cabbage; Net Wt. 24 oz. (1 lb. 8 oz.) 680 g UPC: 0 71430…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dole Fresh Vegetables Inc.
3 more products in this recall
FDA (openFDA food 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.