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 48,122 notices were distributed nationwide, so they reach Virginia too — those are in the archive.
Reported Jul 27, 2016
HX2" Temperature Management Systems; The Terumo¿ HX2" Temperature Management System provides temperature control of two…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 27, 2016
The pump (with cushioning foam inserts) is packaged in a single pump box. Four pump boxes are placed in an over-shipper…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.WalkMed Infusion, LLC
16 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 20, 2016
QuickSlide MGS-80, Automated Mutli-Slide Gram Stainer/GramPRO-80. Systematically stains, rinses, decolorizes, and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hardy Diagnostics
FDA (openFDA device enforcement)
Reported Jul 20, 2016
HeartWare Ventricular Assist System: HeartWare Battery, Lithium Ion, 14.8 V, Rx only. Catalog 1650 (US) and 1650,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Heartware, Inc.
FDA (openFDA device enforcement)
Reported Jul 20, 2016
The LifeCare PCA Plus II infusion pump system is designed for safe, effective, analgesic delivery to patients through…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 20, 2016
Phenylephrine 40 mcg/mL injection in 0.9% Sodium Chloride 10 mL syringe, Rx Only, Compounded by PHARMAKON…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pharmakon Pharmaceuticals, Inc.
87 more products in this recall
FDA (openFDA drug enforcement)
Reported Jul 20, 2016
cobas¿ Liat Influenza A/B Quality Control Kit; For use with cobas¿ Liat Influenza A/B Assay.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Roche Molecular Systems, Inc.
FDA (openFDA device enforcement)
Reported Jul 20, 2016
6.5 mm Cannulated Screw, Product code HWC, Device Listing Number D028949, Screw, Fixation Bone Product Usage: Intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
17 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 20, 2016
Kroger SALAD TOPPERS Roasted & Salted Sunflower Kernels NET WT 3.5 OZ (99G) INGREDIENTS: SUNFLOWER KERNELS, COTTONSEED…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Kroger Co.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 13, 2016
The System 83 Plus, Endoscope Washer/Disinfector Designed for the simultaneous reprocessing of up to two flexible…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Custom Ultrasonics, Inc.
FDA (openFDA device enforcement)
Reported Jul 13, 2016
HeaterBaum Foot & Ankle Heating Pad, Heating Soft Compression Therapeutic Boot with Precise Temperature Control…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ergoactives, LLC
FDA (openFDA device enforcement)
Reported Jul 13, 2016
Magnetic Resonance System G-scan Brio (Part Number /Model No.101002000)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Esaote S.p.A.
FDA (openFDA device enforcement)
Reported Jul 13, 2016
GE Healthcare, Discovery MR750w
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Jul 13, 2016
Item # 4042-CPR Rescue Kit, containing CPR shield with one way valve & barrier filter. brand Lifeline, UPC 845174004429…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lifeline First Aid LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 13, 2016
Synthes Ti Button Plate 7 Holes, Fastener, Fixation, nondegradable, Soft Tissue
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
FDA (openFDA device enforcement)
Reported Jul 13, 2016
Battery Power Line II Battery Oscillator, DePuy Synthes Power Tools, The Anspach Effort Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Anspach Effort, Inc.
FDA (openFDA device enforcement)
Reported Jul 13, 2016
Wegmans Fudgy & Chewy Brownies with Chocolate Chips 14 oz., UPC#7789032990
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wegmans Food Markets, Inc.
6 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 13, 2016
Baby Omega 3 Dietary supplement (in liquid form), 15 ml and 14 ml in glass bottle with dropper dispenser.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Zarbee's Naturals Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 13, 2016
The ZYTO Tower is the input device to program the software with various virtual items.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ZYTO Technologies, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 6, 2016
PrismaSate BGK2/0 Dialysis Solution for Continuous Renal Replacement Therapy
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corp.
FDA (openFDA device enforcement)
Reported Jul 6, 2016
Bigger-Better-Bladder With 3/8" ID tubing, ITEM BBB38
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Circulatory Technology Inc.
FDA (openFDA device enforcement)
Reported Jul 6, 2016
dynarex Specimen Containers, Screw-On, Leak-Resistant Lid, Tamper-Evident Seal, Sterile, Single Use Only Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dynarex Corporation
FDA (openFDA device enforcement)
Reported Jul 6, 2016
MOSAIQ Oncology Information System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jul 6, 2016
Sodium Chloride Inhalation Solution, USP 3%, 60 x 4 mL Sterile Unit-Dose Vials per carton, Rx Only, NDC 0487-9003-60. A…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nephron Pharmaceuticals Corp.
1 more product in this recall
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.