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 11, 2026
MiniMed 780G Insulin Pump Catalog Numbers: MMT-1884 MMT-1886 With Software Version 6.60 The MiniMed 780G insulin pump…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed, Inc.
FDA (openFDA device enforcement)
Reported Feb 11, 2026
Volk Single Use Vitrectomy Lenses 1. Flat Vitrectomy Lens, Catalog VFD 2. Volk Magnifying Lens, Catalog VMD
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vortex Surgical Inc.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 4, 2026
BD Alaris" Pump Module model 8100 UDI-DI code: 10885403810046 The BD AlarisTM System with Guardrails" Suite MX is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Feb 4, 2026
BEAR Implant. Model Number: 1000.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Miach Orthopaedics
FDA (openFDA device enforcement)
Reported Feb 4, 2026
Conductivity Standard Solution Catalog/Model Numbers: 10001, 10011, 10021, 10032, 10040, 10040c, and 10041 Conductivity…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NIPRO Technical Services, Inc.
FDA (openFDA device enforcement)
Reported Feb 4, 2026
Evolution Upgrade 1.5T. Product Codes (REF): (1) 782148, (2) 782116. MR systems with SW version R11.1 and R12.1.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America
12 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 4, 2026
Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle with cap, BIO7771 120 count bottle, BIO7772 120 count…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quten Research Institiute LLC
FDA (openFDA food enforcement)
Reported Feb 4, 2026
Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix R; Siemens Material Number (SMN): 11574002; With Software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 28, 2026
The LDL-Cholesterol assay is comprised of two distinct phases. In phase one a unique detergent solubilizes cholesterol…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Ireland, Inc.
FDA (openFDA device enforcement)
Reported Jan 28, 2026
SQ40S Blood Transfusion Filter
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GVS TM, Inc.
FDA (openFDA device enforcement)
Reported Jan 28, 2026
Tego Connector: REF: 011-D1000, 01C-D1000, 055-D1000, D1000; Conector Tego: REF: LAT-D1000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 28, 2026
Brand Name: Ion Endoluminal System Product Name: Ion Vision Probe Bag Model/Catalog Number: 490127 Software Version:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Jan 28, 2026
Merit Medical Inflation Device.basixCOMPAK.30 atm/bar.20 mL Reference Numbers: ENDO-AN2030/B IN4130/CNK IN4130/H…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 21, 2026
FreeStyle Libre 3 Sensor REF 72081-01 UDI-DI code: 00357599818005 The FreeStyle Libre 3 sensor is a component of the…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abbott Diabetes Care, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 21, 2026
Boston Scientific Coyote OVER-THE-WIRE PTA Balloon Dilation Catheter, 4F, 1) 2.5mm x120mm, 150 cm, UPM/Model No. REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Jan 21, 2026
Brand Name: Catalyst+ Product Name: Catalyst, Catalyst+ Model/Catalog Number: SP001-0026, SP003-0002 Software Version:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C-Rad Positioning Ab
FDA (openFDA device enforcement)
Reported Jan 21, 2026
VANTAGE GALAN 3T Model MRT-3020/MEXL-3020
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 21, 2026
Ivenix Infusion System (IIS), LVP Software: LVP-SW-0005.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Kabi USA, LLC
FDA (openFDA device enforcement)
Reported Jan 21, 2026
2248 Banana Pudding Ice Cream, 3 GAL, UPC 7 65265 81237 8
Moderate riskThis product could cause temporary or reversible health problems — stop using it.House Of Flavors, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 21, 2026
da Vinci SP, SP Access Port Kit, Large Incision Reference Numbers:430073 (2.7-4cm,SP1098, Box) & 430075…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Jan 21, 2026
Medicrea, IB3D Universal Implant Inserter, Rx Only REF: A24000000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medicrea International
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 21, 2026
Detachable 10in Pend FRU-1 Pend component for the AIRO Computed Tomography (CT) X-ray System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mobius Imaging, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 21, 2026
CentriMag Blood Pump, REF: 102953, 201-20003, 201-90010, 201-90016; CentriMag RVAD HDE KIT, REF: 104318; CentriMag…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec LLC
FDA (openFDA device enforcement)
Reported Jan 21, 2026
Ukrop's 6" Pound Cake with Buttercream Icing/Confetti NET WT 30 OZ (1.88lb/851g) CONTAINS: Egg, Milk, Wheat Made in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ukrop's Homestyle Foods, LLC
2 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.