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 18, 2022
OnGuard2 CSTD Bag Adaptor SP A Chemfort CSTD Product, Product code MG412143
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Simplivia Healthcare Ltd.
FDA (openFDA device enforcement)
Reported May 18, 2022
12/5 oz. bags of O-Organic Sea Salt Popcorn. UPC Code: 79893403038
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Snak King Corporation
FDA (openFDA food enforcement)
Reported May 13, 2022
FSIS Issues Public Health Alert for Weis Markets’ Ready-To-Eat General Tso Chicken Meals Due to Misbranding and…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Fsis
USDA FSIS
Reported May 11, 2022
Olive; TOP SAVOR Licorice Flavored Olive; Net wt: 500g (17.63oz); Ingredients: olive, sugar, salt, licorice extract,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.A & C Best Food Trading
2 more products in this recall
FDA (openFDA food enforcement)
Reported May 11, 2022
Non-Sterile Double Ended Trial Kit, Small Footprint, (6110-N01-KTS01) for the Cervical Cage. The kit includes 3 trials.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.restor3d Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 7, 2022
Wayne Farms, LLC Recalls Ready-To-Eat Chicken Breast Fillet Products That May Be Undercooked
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wayne Farms LLC
USDA FSIS
Reported May 4, 2022
ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carl Zeiss Meditec AG
FDA (openFDA device enforcement)
Reported May 4, 2022
Kinder Happy Moments Kinder Chocolate and Crispy Wafers Assortment 14.1 OZ (400g) square box with lid. Best by: July…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ferrero USA Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 4, 2022
da Vinici X da Vinci Xi Sureform 45 REF 480445 da Vinci X da Vinci Xi Sureform 45 Curved-Tip REF 480545 da Vinici X da…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported May 4, 2022
MEDTRONIC INTERSTIM THERAPY SYSTEM FOR URINARY CONTROL, which includes the following: a) Handset with Communicator,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported May 4, 2022
NeuMoDx Cartridge-For in vitro diagnostic use with NeuMoOx Molecular Systems with either of the following assays:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NeuMoDx Molecular Inc.
FDA (openFDA device enforcement)
Reported May 4, 2022
IMMULITE 2000 Systems HCG [200 Tests, material number 10381206, catalog number L2KCG] and [600 Tests, material number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported May 4, 2022
syngo.via RT Image Suite upgraded to VB60 running on syngo.via Model Number 10496180. Running on servers with syngo.via…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 4, 2022
TearCare version 1.0 SmartHubs
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sight Sciences, Inc.
FDA (openFDA device enforcement)
Reported May 3, 2022
Safeway Fresh Food, LLC Recalls Ready-To-Eat Salad Containing Chicken Due to Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.Safeway Fresh Food, LLC
USDA FSIS
Reported Apr 27, 2022
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Yellow, REF H93866100, 100 slip tip caps/package.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Apr 27, 2022
ORAcollect Dx, Catalog Number/SKU: OCD-100, OCD-100A. Material numbers: OCD-100, OCD-100.008, OCD-100.012,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DNA Genotek Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 27, 2022
HUNTLEIGH Disposable intraoperative Probe, 8Mhz (box), REF DIPP10, containing 10 individual Disposable Intraoperative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Huntleigh Healthcare Ltd.
FDA (openFDA device enforcement)
Reported Apr 27, 2022
Matrix Clinical Solution At-Home COVID-19 Test
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Matrix Medical Network
FDA (openFDA device enforcement)
Reported Apr 27, 2022
Philips Respironics V60 Ventilator (All Models, including: 1053613, 1053614, 1053615, 1053616, 1053617, 1053618,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Respironics California, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 27, 2022
Merlin PCS 3650 programmer Model 3330 software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St. Jude Medical, Cardiac Rhythm Management Division
4 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 22, 2022
Tennessee Brown Bag, LLC Retira Productos De Carne Seca Producidos Sin El Beneficio De La Inspección
High riskUsing this product could cause serious injury, illness or death — stop using it now.Recalling firm not stated
USDA FSIS
Reported Apr 20, 2022
20/30 INDEFLATOR -REF 1000184 WPL2122268-01 (2019-03-01)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Vascular
4 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2022
NATURE's ANSWER Coral Calcium; Antioxidant Benefits*; 1000mg Coral Calcium per serving; DIETARY SUPPLEMENT; 90 capsules
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Botanica, Inc.
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.