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 Aug 12, 2026
Neuroguard IEP 3 in 1 Carotid Stent and Post-Dilation Balloon System with Integrated Embolic Protection (Neuroguard IEP…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Contego Medical, Inc.
FDA (openFDA device enforcement)
Reported Aug 12, 2026
GEM Premier 7000 with iQM3 Part Numbers: 00077407508 00077407510 00077415004 00077415008 00077415010 00077430010…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumentation Laboratory
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 12, 2026Updated Sep 16, 2026
Oribe Serene Scalp Densifying Shampoo, packaged in 8.5 fl. oz. (250 mL) bottles with UPC 840035231242 and 33.8 fl. oz.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.KAO USA Inc.
FDA (weekly enforcement report)
Reported Aug 12, 2026
La Colonia Foods Salvadoreno Requeson Soft Ricotta, Net Wt: 14 oz (367g), packaged into retail-sized clear plastic…
High riskUsing this product could cause serious injury, illness or death — stop using it now.La Colonia Foods LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 12, 2026
Spicy Breakfast Burrito sold under the following brand names: FRESH & READY FOODS Spicy Breakfast Burrito Net Wt. 8.2…
High riskUsing this product could cause serious injury, illness or death — stop using it now.M.G. Foods, Inc.
FDA (openFDA food enforcement)
Reported Aug 12, 2026
Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40 6677400 Flow-i C20 6888520 Flow-i C30 6888530…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Critical Care AB
FDA (openFDA device enforcement)
Reported Aug 12, 2026
Brand Name: OXOS Medical, Inc Product Name: MC2 Portable X-Ray System Model/Catalog Number: MC2, MC2.1 Software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oxos Medical Inc.
FDA (openFDA device enforcement)
Reported Aug 12, 2026
Brand Name: Quantum Rehab Product Name: Quantum 4Front 2 Model/Catalog Number: Quantum 4Front 2 Software Version:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pride Mobility Products Corp.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 12, 2026
Pumpkin Tree Peter Rabbit Organics Banana & Strawberry fruit puree, 4oz/113g pouch, UPC 815367010780, PTO Item 10720.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PT Organics Limited
FDA (openFDA food enforcement)
Reported Aug 12, 2026
Syva Emit Disopyramide Assay Enzyme Immunoassay, Lidocaine SMN 10445370 Catalog No 6N319UL
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Siemens Healthcare Diagnostics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2026
L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga (1.9F) 0.60mm x 30cm, REF: 384539; 18ga (3.5F) 1.15mm x…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Argon Medical Devices, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2026Updated Sep 16, 2026
Sainforage Sainfoin + Grass + Alfalfa Forage Pellet 40 lb (18.14 KG) UPC: 720260672693. Packaged BOPP woven plastic…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fundamental Feed
2 more products in this recall
FDA (weekly enforcement report)
Reported Aug 5, 2026
Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Permobil Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2026
Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides continuous or intermittent ventilatory…
High riskUsing this product could cause serious injury, illness or death — stop using it now.ResMed Ltd.
FDA (openFDA device enforcement)
Reported Aug 5, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 30mm. Catalog Number: 50796030.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker GmbH
6 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2026
AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) ENT Pack, Part Number AMS10411B; 2) ENT Pack,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Windstone Medical Packaging, Inc.
11 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 31, 2026Updated Aug 25, 2026
Ukrop's Homestyle Foods Recalls Spaghetti and Chicken Products Due to Possible Foreign Matter Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ukrop's Homestyle Foods
USDA FSIS
Reported Jul 29, 2026
Power F2 Powered Fastening System, Product No. 0567091 Powered fastening system intended for professional use only.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ferno-Washington Inc.
FDA (openFDA device enforcement)
Reported Jul 29, 2026
Flexible Hystero-Fiberscope Kits REF: 11264BBU1, 11264BBUK1, that contain expired Single Use Endoscopic Seal: GYN, REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
FDA (openFDA device enforcement)
Reported Jul 29, 2026
MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed, Inc.
FDA (openFDA device enforcement)
Reported Jul 29, 2026
Pipeline Flex Embolization Device with Shield Technology, 3.00 mm x 12 mm 027 REF PED2-300-12. Intracranial aneurysm…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Micro Therapeutics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2026
Penumbra System RED 68 Reperfusion Catheter REF: RED68KIT
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Penumbra, Inc.
FDA (openFDA device enforcement)
Reported Jul 29, 2026
Brand Name: Silent Nite Product Name: Silent Nite Sleep Appliance Model/Catalog Number: SILNT Product Description:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Prismatik Dentalcraft, Inc.
FDA (openFDA device enforcement)
Reported Jul 29, 2026
SeaSpine Polyaxial Head REF Number: 41-3010
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Seaspine Orthopedics Corporation
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.