All recall categories

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.

Food

Reported Jan 8, 2025

Sprout Gyro Family Kit, net wt. 1.750 lb (794 g), food, perishable, plastic tray, 28oz, U UPC 20594800000.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Sprouts Farmers Market

FDA (openFDA food enforcement)

Medical devices

Reported Jan 1, 2025

The Merlin PCS 3650 programmer Model 3330 The Merlin PCS programmer model 3650 is a portable, dedicated programming…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Medical

FDA (openFDA device enforcement)

Medical devices

Reported Jan 1, 2025

20/30 INDEFLATOR, REF: 1000184, for use during cardiovascular procedures in conjunction with interventional devices…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Vascular Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 1, 2025

FACSLyric 2L4C Instrument US, Catalog Number 662875, UDI 00382906628756 BD FACSLyric" flow cytometer is intended for in…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton, Dickinson and Company, BD Bio Sciences

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 1, 2025

BORSARI Food Company Incorporated; BLOODY MARY MIX ; 32 FL. OZ; INGREDIENTS: Tomato juice, corn syrup, non-fat milk…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Borsari Food Company Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 1, 2025

MISHA Knee System Implant Small, Left, REF: 2-1001. MISHA Knee System Implant Small, Right, REF: 2-1002.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Moximed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 1, 2025

Brand Name: Daytona Small Stature Product Name: CoCr LockingCap 4.5mm, Small Stature, T25, BT Model/Catalog Number:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Seaspine Orthopedics Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 1, 2025

BYTE Aligner System REF PRS-0063 BYTE All-Day Aligner System BYTE AT-Night Aligner System A custom-made orthodontic…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Straight Smile, LLC

FDA (openFDA device enforcement)

Food

Reported Jan 1, 2025

ZOE brand Daily 30+ Prebiotic blend; Dietary Supplement; 500g resealable pouch

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zoe US, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 25, 2024

Brand Name: K-Systems Product Name: G73 Dry Bath Incubator Model/Catalog Number: K22065 Product Description: An…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CooperSurgical, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 25, 2024

Fabalish Inc. , Kickin, Carrot Falafel , 10oz , Cardboard tray inside plastic film inside cardboard box, individual…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Fabalish,

FDA (openFDA food enforcement)

Medical devices

Reported Dec 25, 2024

OEC 3D REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The OEC 3D is a mobile fluoroscopic C-Arm imaging…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE OEC Medical Systems, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 25, 2024

Galaxy System (GAL-001)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Noah Medical

FDA (openFDA device enforcement)

Medical devices

Reported Dec 25, 2024

Eclipse PRO REF 98700 The Spacelabs model 98700 is a portable non-invasive Holter recorder intended to record the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Spacelabs Healthcare, Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 25, 2024

Turbo Elite Laser Atherectomy Catheter Model Number / UDI-DI code / Product Description 414-151 / 989930000531 / 1.4 mm…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Spectranetics Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2024

BD Pyxis MedStation ES, REF: 323

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 18, 2024

DesBio lunaSOMM Natural Sleep Support Dietary Supplement capsules, 30 count in a Blue PET bottle with a White cap.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Deseret Biologicals Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 18, 2024

Hybrid Recon software on Hermes Medical Imaging Suite version 6.1 Hybrid Recon software versions affected are 4.0.0x…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hermes Medical Solutions AB

FDA (openFDA device enforcement)

Food

Reported Dec 18, 2024

"***SUPER***BRAND***DRIED CINNAMON POWDER***Net Wt: 4oz(113g)***PRODUCT OF CHINA***DISTRIBUTOR: IHA BEVERAGE COMMERCE,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Kim-Seng Company

FDA (openFDA food enforcement)

Food

Reported Dec 18, 2024

Nestle Health Services Nutren 2.0 kCal/mL, Calorically Dense Complete Nutrition with Fiber Unflavored. 1000mL (1.1QT).…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Nestle Health Science

FDA (openFDA food enforcement)

Food

Reported Dec 18, 2024

Fresh Gourmet TORTILLA STRIPS SANTA FE SYTLE NET WT 3.5 OZ (99g) UPC 7 87359 17504 6 DISTRIBUTED BY: FRESH GOURMET CO.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Sugar Foods LLC

FDA (openFDA food enforcement)

Food

Reported Dec 18, 2024

Jarritos Coconut Water 17.5 fl oz cans- 12 cans per carton

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Tipp Distributors, Inc. dba Novamex

FDA (openFDA food enforcement)

Medical devices

Reported Dec 11, 2024

Hollister CalciCare Calcium Alginate Dressing REF 529937R calcium alginate dressings are indicated for moderate to…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Advanced Medical Solutions Ltd.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 11, 2024

OneMultivitaminic GAF-PLUS Advance 300ml, plastic bottle, Room Temperature

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Armonia Natural Store LLC

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.