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 48,123 notices were distributed nationwide, so they reach Virginia too — those are in the archive.

Medical devices

Reported May 16, 2018

PICC Kit, Product Code: AMS-7063-1 Convenience kit for the insertion of PICCs into the vascular system.

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

Vygon U.S.A.

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 9, 2018

Alere iScreen Dx Urine Drug Screen Card

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Ameditech Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 9, 2018

BD MAX DNA MMK (SPC) For Laboratory Use, catalog no. 442829

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Becton Dickinson & Co.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported May 9, 2018

Happy Harvest Leaf Spinach; Net Wt. 13.5 oz (383g); Ingredients: Spinach, Water, Salt. Distributed by Aldi Inc.…

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

Mccall Farms Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 9, 2018

Allura Xper R8.x.25.5 and UNIZ systems (only with a FlexVision large screen monitor), Interventional fluoroscopic x-ray…

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

Philips Electronics North America Corporation

FDA (openFDA device enforcement)

Medical devices

Reported May 9, 2018

PTS Panels¿ CHOL+GLU Test Strips (REF 1765)

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

Polymer Technology Systems, Inc.

FDA (openFDA device enforcement)

Food

Reported May 9, 2018

Chocolate Sea Salt Probiotic Granola, Purely Elizabeth, 8oz, PET/LLDPE Pouch, 6 units/case,

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

purely elizabeth.

FDA (openFDA food enforcement)

Food

Reported May 9, 2018

Protein key brand Protein Meals varieties, 2.5 lb plastic container and 400 g plastic container, Varieties: Anti-Aging…

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

Wysong Corporation

24 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 9, 2018

Modular Head Component, Biomet Hip System; Item No. 163669, Hip Joint, metal/polymer semi-constrained cemented…

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

Zimmer Biomet, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 2, 2018

clariti 1 day/Fresh Day 90 pack (-1.00), UV Blocking, 90 silicon hydrogel, daily disposable contact lenses The Clariti…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

CooperVision Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 2, 2018

EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 3.5MM, Product Number HEM3335, GTIN Number 1 -…

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

Covidien LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 2, 2018

Triathlon Revision Knee Catalog #5545-A-301 and Catalog #5546-A-601 The knee system devices are sterile, single-use…

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

Howmedica Osteonics Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 2, 2018

Proteus 235, ProteusPLUS or Proteus ONE produces and delivers a proton beam for the treatment of patients with…

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

Ion Beam Applications S.A.

FDA (openFDA device enforcement)

Medical devices

Reported May 2, 2018

Oncomine Dx Target Test, (Model No. A32451), Oncomine Dx Target RNA/DNA Panel (Model No. A32441). A qualitative In…

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

Life Technologies Corporation

FDA (openFDA device enforcement)

Food

Reported May 2, 2018

Nxtgen Botanicals, Maeng Da Kratom, Dietary Supplement, 70 capsules

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

NGB, Corp.

FDA (openFDA food enforcement)

Food

Reported May 2, 2018

Shell Eggs packaged in quantities and styles of pack (plastic and pulp cartons, flats, and boxes)

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

Rose Acre Farm

FDA (openFDA food enforcement)

Medical devices

Reported May 2, 2018

Versatex Monofilament Mesh 50 x 50cm, Product No. VTX5050M The device is made out of a macroporous three-dimensional…

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

Sofradim Production

FDA (openFDA device enforcement)

Meat & poultry

Reported May 2, 2018

JBS USA, Inc. Recalls Ground Beef Products Due to Possible Foreign Matter Contamination

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

Swift Beef Company

USDA FSIS

Food

Reported Apr 25, 2018

Kratom capsules labeled in the following ways: 1) Divinity Kratom 10 Capsule Dietary Supplement, Divinity Product LLC,…

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

Divinity Product Distribution LLC

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Apr 25, 2018

SANTA CRUZ organic APRICOT fruit spread NET WT 9.5 OZ (270 g) UPC 0 36192 10514 8

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Smucker Natural Foods, Inc.

5 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Apr 25, 2018

Dr. Pepper Est. 1885 Diet, 20 FL Oz (1.25 PT), 591 mL

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

Swire Coca Cola USA

FDA (openFDA food enforcement)

Food

Reported Apr 25, 2018

HUNGRY JACK Original PANCAKE & WAFFLE MIX NET WT 32 OZ (2 LB) 907 g

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

The J.M. Smucker Company, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 25, 2018

Zimmer Segmental System Proximal Femoral Component 38mm Offset, Model Number 00-5850-030-38 The Segmental System is…

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

Zimmer Biomet, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 18, 2018

First aid/emergency kits containing Honeywell eyewash: CSM kit number Kit/cabinet Description CSM Eyewash# Size:…

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

Certified Safety Mfg Inc.

FDA (openFDA device enforcement)

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Other states

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.