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 Dec 14, 2016
Halyard C-Section Drape with Clear Screen and Full Incise (Non-Sterile), Product Code 44965 NS; C-Section Drape with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Halyard Health, Inc.
FDA (openFDA device enforcement)
Reported Dec 14, 2016
Meijer Almonds Salted Caramel, 14 oz. packaged in plastic pouches
High riskUsing this product could cause serious injury, illness or death — stop using it now.Meijer, Inc.
FDA (openFDA food enforcement)
Reported Dec 14, 2016
Dai Yu, 80g, Hairtail, NET WT: 2.8 oz (80g), Item #D526
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Midwest International Corp.
FDA (openFDA food enforcement)
Reported Dec 14, 2016
Premium Norwegian Salmon, Smoked, slice 8oz (227g), UPC # 856687004288, Keep refrigerated
High riskUsing this product could cause serious injury, illness or death — stop using it now.Olma-Xxi Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 14, 2016
Olympus Scientific Solutions Americas Corporation ( OSSA ) Model: VANTA Analytical X-Ray System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Scientific Solutions Americas
FDA (openFDA device enforcement)
Reported Dec 14, 2016
Barbiturates Intercept Micro-Plate EIA (enzyme immunoassay, barbiturate) Product is intended for use by clinical…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.OraSure Technologies, Inc.
FDA (openFDA device enforcement)
Reported Dec 14, 2016
Homestyle Texas Toast. 1 lb. 8 oz. Clear Plastic Bag. 1 loaf
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pastian's Bakery
7 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 14, 2016
Airheads Mini Bars 12oz bags of assorted flavors. 12 - 12oz bags are included in cardboard cartons. Assorted flavors…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Perfetti Van Melle USA Inc.
FDA (openFDA food enforcement)
Reported Dec 14, 2016
Brilliance 64 728231 Computed Tomography X-ray systems intended to produce cross-sectional images of the body by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 14, 2016
Salted Caramel Almonds
High riskUsing this product could cause serious injury, illness or death — stop using it now.R & J Almonds, Inc. dba Jonny Almond Nut Co.
FDA (openFDA food enforcement)
Reported Dec 14, 2016
Perceval Sutureless Aortic Heart Valve size S, Item # ICV1208, REF PVS21; Perceval Sutureless Aortic Heart Valve size…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sorin Group USA, Inc.
FDA (openFDA device enforcement)
Reported Dec 14, 2016
5000 Series Freedom Drivers. Freedom Driver System for Temporary Total Artificial Heart (TAH-t). Part number 595000-001
High riskUsing this product could cause serious injury, illness or death — stop using it now.SynCardia Systems Inc.
FDA (openFDA device enforcement)
Reported Dec 14, 2016
MANOS EX (CAT#TY-12-101) Product Usage: Carpal Tunnel Release: as a tool for tissue release of the transverse carpal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thayer Intellectual Property, Inc.
FDA (openFDA device enforcement)
Reported Dec 7, 2016
FMsealer Open Shears. Model FM3001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Domain Surgical, Inc.
FDA (openFDA device enforcement)
Reported Dec 7, 2016
Monaco RTP System; Used to make treatment plans for patients with prescriptions for external beam radiation therapy.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 7, 2016
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)
Reported Dec 7, 2016
MSS CASSETTE GLU/LAC/UREA (BUN) as a part of the Roche OMNI S Analyzer: cobas b 221<6>Roche OMNI S6 system The Roche…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Dec 7, 2016
Adiprep Adipose Transfer System. Product Codes: 51431; 51432; 51433; 514001-347.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo BCT, Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2016
COBRA Fusion 50 Ablation System, COBRA Fusion 150 Ablation System, and COBRA Fusion Magnetic Retriever System. Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AtriCure, Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2016
BM Westco Mster Mix Raised Donut Mix, 50#
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CSM Bakery Products NA
21 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 30, 2016
ACTIS Flex Reamers SZ 0/1; 2/3; 4/5; 6/7; 8/9; 10/11; 12, Product is sold non-sterile, these instruments are packed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Depuy Orthopaedics Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2016
DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-DRILLING SCREW 4.0 x 18mm Item Code: 186850018 The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Spine, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 30, 2016
Protein Chews Cherry Lime,1.8oz, film package, 12 packets per box.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.EN-R-G Foods, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 30, 2016
Simeons Program. 2oz HCG Drops. Amber Plastic.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Infiniti Creations, LLC
18 more products in this recall
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.