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 Feb 5, 2025
Medtronic PIN, 100mm STERILE PERCUTANEOUS REF: 9733235 Medtronic PIN, 150MM, STERILE PERCUTANEOUS REF: 97733236 The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Jan 29, 2025
Baxter Solution Set with Duo-Vent Spike, REF 2R8404
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 29, 2025
BD PCR Cartridges used with MAX System. Model Number: 437519
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Jan 29, 2025
CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model Number: 828810 Implantable device that provides…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 29, 2025
Brand Name: N/A Product Name: Repeater Bone Tamp Model/Catalog Number: ASY-00132 Software Version: N/A Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integrity Implants Inc.
FDA (openFDA device enforcement)
Reported Jan 29, 2025
Buttered Vegetables KEEP FROZEN NET WT 10.5 OZ (300g) INGREDIENTS: CARROTS, PEAS, CALIFLOWER, CORN, BUTTER, SUGAR,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lidl US TRADING
FDA (openFDA food enforcement)
Reported Jan 29, 2025
Brand Name: HALYARD Product Name: Laparotomy Pack Model/Catalog Number: 88231 Software Version: N/A Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.O&m Halyard, Inc.
FDA (openFDA device enforcement)
Reported Jan 27, 2025
FSIS Issues Public Health Alert for Wegmans Frozen Fully Cooked Chicken Nuggets Due to Possible Extraneous Material…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Perdue Foods LLC
USDA FSIS
Reported Jan 22, 2025
VerifyNow P2Y12 Platelet Reactivity Test, REF: 85064
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Accriva Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Jan 22, 2025
Brand Name: Alcon Product Name: Monarch¿ III D Delivery Cartridge Model/Catalog Number: 8065977763 Product Description:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 22, 2025
8MM, MONOPOLAR CURVED SCISSORS, IS4000 REF 470179
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
38 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 22, 2025
Karl Storz - Endoskope - REF 723400 - Optical Biopsy and Grasping Forceps, CE
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
FDA (openFDA device enforcement)
Reported Jan 22, 2025
Neo-Tee T-Piece Resuscitator, for pediatric emergency respiratory support, Part: 1050805, 1050808, 1050809, 1050810,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mercury Enterprises, Inc. dba Mercury Medical
FDA (openFDA device enforcement)
Reported Jan 22, 2025
Yu Yee, Five Spice Powder,1.76oz
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Summit Import Corporation
FDA (openFDA food enforcement)
Reported Jan 15, 2025
Aerin Medical VivAer Stylus, REF CAT1785 (individual stylus), and REF CAT500 (5-pack), sterile.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aerin Medical, Inc.
FDA (openFDA device enforcement)
Reported Jan 15, 2025
AMT Mini Enteral Extension Set, 12" Right Angle Feeding Set with Y-Port. Model/Catalog Number: E6-1222
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Applied Medical Technology Inc.
FDA (openFDA device enforcement)
Reported Jan 15, 2025
235214 Baker's Source Traditional Cornbread Mix Complete, 5 LB Bags, 30 LB Cases Foodservice Use, Human Consumption &…
High riskUsing this product could cause serious injury, illness or death — stop using it now.C.H. Guenther & Son, Inc.
FDA (openFDA food enforcement)
Reported Jan 15, 2025
Ivenix Infusion System (IIS), Large Volume Pump, Model Number: LVP-0004
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fresenius Kabi USA, LLC
FDA (openFDA device enforcement)
Reported Jan 15, 2025
Grecian Delight Tzatziki sauce, 3.75 lb. tub, UPC 07365000286, SKU SAL028, 4 tubs per case. Sysco Classic Tzatziki…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Grecian Delight/Kronos
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 15, 2025
The FastPack IP Sex Hormone Binding Globulin Immunoassay, Part #25000081, is for the quantitative measurement of SHBG…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Qualigen Inc.
FDA (openFDA device enforcement)
Reported Jan 15, 2025
Xhibit Telemetry Receiver, Model 96280, with Service Manual. Intended to provide monitoring system with patient data.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 8, 2025
3M Unitek Transbond Plus Self-Etching Primer REF 712-090 (100 unit box) 712-091 (20 unit box) Transbond Plus Self…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.3M Unitek Corporation
FDA (openFDA device enforcement)
Reported Jan 8, 2025
AURYON LASER SYSTEM 100-120 VAC. Model Number: EXM001. Product Number: EXM-2001-1100
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics, Inc.
FDA (openFDA device enforcement)
Reported Jan 8, 2025
--- Organic Baby Carrots --- Organic Baby Peeled Carrots 12/12oz Steam-to-Serve; Organic Baby Peel Carrot12/12oz…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Grimmway Enterprises, Inc. dba Grimmway Farms
4 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.