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 May 1, 2024
ACUSON Juniper Diagnostic Ultrasound System, REF: 11335791, and ACUSON Juniper Select Diagnostic Ultrasound System,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 1, 2024
NexGen CR-Flex Femoral Component, Size E and Size E Minus (E-). Component of the NexGen CR-Flex Porous Femur System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Apr 24, 2024
ConSup North America Inc. Recalls Ready-To-Eat Sliced Prosciutto Product Produced Without Benefit of Inspection
High riskUsing this product could cause serious injury, illness or death — stop using it now.ConSup North America Inc.
USDA FSIS
Reported Apr 24, 2024
Masimo Rad-G, Pulse Oximeter with temperature (W/Sensor), REF:9210, Rx Only,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Masimo Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 24, 2024
Tablo Hemodialysis System, REF: PN-0003000, PN-0006000 and PN-0007001
High riskUsing this product could cause serious injury, illness or death — stop using it now.Outset Medical, Inc.
FDA (openFDA device enforcement)
Reported Apr 24, 2024
AW-S025 NEO SONARMED SENSOR 2.5MM. Used in conjunction with SonarMed Monitor for airway monitoring.
High riskUsing this product could cause serious injury, illness or death — stop using it now.SonarMed Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 24, 2024
Helados Mexico Premium Ice Cream Minis Variety Pack 12 bars Strawberry, Coconut, Mango 1.5 FL OZ (44mL) Bards Net 18 FL…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Tropicale Foods, Inc.
FDA (openFDA food enforcement)
Reported Apr 17, 2024
LVP Software of the Ivenix Infusion System (IIS), Version 5.8.0.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fresenius Kabi USA, LLC
FDA (openFDA device enforcement)
Reported Apr 17, 2024
Patient Cart, Part: 380601, a component of the da Vinci SP Surgical System, Model: SP1098
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Apr 17, 2024
Deluxe brand Macarons Party Edition 35 pieces 455g (35 x 13g) UPC:4056489365365 Product packaged in a cardboard/plastic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lidl US TRADING
FDA (openFDA food enforcement)
Reported Apr 17, 2024
SWAD BRAND CINNAMON POWDER in clear plastic 3.5 OZ bags, UPC 0-51179-34280-4, 20 retail units per wholesale case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raja Foods LLC
FDA (openFDA food enforcement)
Reported Apr 17, 2024
Egg salad sandwich packaged in clamshell for individual sale. 7.22oz (205g) UPC 766375938415
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Coastal Companies dba Hearn Kirkwood
FDA (openFDA food enforcement)
Reported Apr 17, 2024
Whitley's Peanut Factory, Deluxe Nut Mix, 12oz (340g), Electrolytic tin-plated cans, with paper label. 12-pack case…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Whitley Peanut Factory, Inc.
FDA (openFDA food enforcement)
Reported Apr 10, 2024
3M Tube Securement Device, Small, 1.7 IN/PO x 2.4 IN/PO, REF 1500U, Sterile; and 3M Tube Securement Device, Large, 2.2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.3M Company - Health Care Business
FDA (openFDA device enforcement)
Reported Apr 10, 2024
ARCHITECT STAT Myoglobin Reagent Kit, LN 2K43-25 and 2K43-20.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
FDA (openFDA device enforcement)
Reported Apr 10, 2024
AJI MORI***CHILLIMAMI SAUCE***UMAMI BOMB***NET WT. 250ml. Packaged in a LDPE bottle. Refrigerate after opening.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aji Mori Sauce Corp.
FDA (openFDA food enforcement)
Reported Apr 10, 2024
Karl Storz SE & CO. KG, REF 11003MB, Grasping Forceps, Flexible 1 mm, Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 10, 2024
Sekeroglu Lokum Love Turkish Delight Mixed With Pistachio And Pomegranate Flavor Wrap Delight 350 grams…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Turkana Food Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 3, 2024
Epix Universal Clip Applier, REF: CA500, STERILEEO
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Applied Medical Resources Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 3, 2024
Barsotti Organic Carrot Juice 16 oz. and 64 oz. plastic bottles Perishable, Keep Refrigerated Ingredient: Fresh Pressed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Barsotti Juice Company, Inc.
FDA (openFDA food enforcement)
Reported Apr 3, 2024
Baxter Peri-Guard Repair Patch (legacy product codes): a) PC0404NBIO, b) PC0608NBIO, c) PC0814NBIO, d) PC1016NBIO
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 3, 2024
O.T.D - Optimum Traction Device - Street Orange. Single use traction splint.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Emergency Products & Research
FDA (openFDA device enforcement)
Reported Apr 3, 2024
Medivance Neonatal ArcticGel Pads, REF: 31802, 3180202, 31802C
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medivance Inc.
FDA (openFDA device enforcement)
Reported Apr 3, 2024
HydroFlock Sterile Flocked Collection Device, Part Number 25-3317-H.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Puritan Medical Products Company, LLC
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.