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 Apr 20, 2022
LIPOSORBER System, Model: LA-15, consisting of: Apheresis machine, product# 101445 model: MA-03, and disposables…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kaneka America Corp.
FDA (openFDA device enforcement)
Reported Apr 20, 2022
Hydroxybutyrate LiquiColor Tests - includes 3 bottles (1 of each size, 3mL, 8.5mL, and 50mL)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MEDLINE INDUSTRIES, LP - Northfield
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2022
Access-9 Large Bore Hemostasis Valves, Catalog Code: 580775001, IN8112/C, K05-00053H, K05-00109G, K05-00137K,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2022
Cub 2 Enclosed Bed Canopy System
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sensory Medical Inc.
FDA (openFDA device enforcement)
Reported Apr 20, 2022
ARIA Radiation Therapy Management (RTM) VERSIONS 13.6, 15.1, 15.5, 15.6, 16.0, 16.1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Varian Medical Systems Imaging Laboratory GmbH
FDA (openFDA device enforcement)
Reported Apr 13, 2022
Alinity m HBV Application Specification File (US and CE)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Molecular, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 13, 2022
Panther Fusion GBS Assay Cartridges 96 Tests, Catalog Number: PRD-04484. in vitro diagnostic test for group b…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hologic, Inc.
FDA (openFDA device enforcement)
Reported Apr 13, 2022
Cardiohelp-i Transport Guard with Transport Guard (701072525): is a blood oxygenation and carbon dioxide removal system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Medical Systems USA
FDA (openFDA device enforcement)
Reported Apr 13, 2022
Caesar dressing in a 1.5 oz pouch
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Sauer Brands Inc. - New Century
FDA (openFDA food enforcement)
Reported Apr 13, 2022
BenchMark ULTRA and DISCOVERY ULTRA Instruments
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ventana Medical Systems Inc.
FDA (openFDA device enforcement)
Reported Apr 13, 2022
SyncVision Systems, Model: 400-0100.10, PN: 30000485688x, with software version 4.2.x
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Volcano Corporation
FDA (openFDA device enforcement)
Reported Apr 6, 2022
Liko Universal Twinbar 670 QRH, an accessory that can be used together with most Liko lifts, model numbers 3156087 and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2022
(a) CareFusion Snowden-Pencer Plastics, Endoplastic Endoscope 10 mm, 30 degrees 7", 17.5 cm, Catalog #88-5910; (b)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carefusion 2200 Inc.
FDA (openFDA device enforcement)
Reported Apr 6, 2022
FORE-SIGHT ELITE Absolute Tissue Oximeter, REF: 01-06-3000, Contents: Monitor 1 EA., Accessory Kit 1 EA.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2022
Hanger-Bar 2P 45cm
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Human Care USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2022
Illumina NextSeq 550Dx, REF: 20005715, CE, IVD
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Illumina, Inc.
FDA (openFDA device enforcement)
Reported Apr 6, 2022
MiniMed 630G: MMT-1715, MMT-1754, MMT-1755; MiniMed 670G: MMT-1740, MMT-1741, MMT-1742, MMT-1760, MMT-1761, MMT-1762,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed
FDA (openFDA device enforcement)
Reported Apr 6, 2022
Revogene, For In Vitro Diagnostic use in performing nucleic acid testing in clinical laboratories. Meridian branded…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Meridian Bioscience Inc.
FDA (openFDA device enforcement)
Reported Apr 6, 2022
RayStation 4-11B, and RayPlan 1, 2, 7-11B including some service packs: RayStation 4.0 (4.0.0.14) to RayStation 5…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RaySearch America Inc.
FDA (openFDA device enforcement)
Reported Apr 6, 2022
Siemens Dimension Vista Magnesium Flex reagent cartridge (MG) Material # 10445158, Catalog # K3057 used in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Apr 6, 2022
Good & Gather Dried Sweetened Strawberries. Net Wt 4 oz (113g). UPC 085239-182840 No Sulfites Added. No Artificial…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Suntree Snack Foods, LLC
FDA (openFDA food enforcement)
Reported Mar 30, 2022
NuOss Collagen Block Size 8mm x 9mm x 9mm- used in filling periodontal and maxillofacial defects. Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ace Surgical Supply Co., Inc.
FDA (openFDA device enforcement)
Reported Mar 30, 2022
Flow Alkaline Spring Water - Organic lemon & ginger flavored water. 500 ml 12 units per case . Tetra Pak paper carton.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Flow Beverages Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Mar 30, 2022
Outset Tablo Console Model Number: PN-0003000 Model Number: PN-0006000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Outset Medical, Inc.
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.