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 Mar 7, 2018
Agility with Integrity R3.2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta Limited
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 7, 2018
Ultrasound Transducer, Model Number: UST-5550-R, is used in conjunction with a diagnostic ultrasound system evaluation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported Mar 7, 2018
Footswitch accessory to the CUSA Clarity Ultrasonic Tissue Ablation System; Catalogue No: C7000 Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Mar 7, 2018
Max Implant System - Bone Tap for use with 7.0mm diameter Max Implant, Catalog Number D-TAP-MAX7-7 Dental implants are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Keystone Dental Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 7, 2018
M&P Food Productions brand Vareniki, Potato and Mushroom, Net Wt. 14 oz. (396 g), Keep Frozen, UPC: 7 07163 02617 4
Moderate riskThis product could cause temporary or reversible health problems — stop using it.M & P Food Productions, Ltd.
6 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 7, 2018
Meijer Greek Yogurt 0% Black Cherry 5.3 oz. The products are packaged in a plastic cup with a foil seal and a label…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Meijer Distribution, Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 7, 2018
AIRO Mobile CT System, Model Number: MobiCT-32 Product Usage: The AIRO¿ is intended to be used for X-ray computed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mobius Imaging, LLC
FDA (openFDA device enforcement)
Reported Mar 7, 2018
OTTO BOCK Kenevo knee joints Model 3C60
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Otto Bock Healthcare Product
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 7, 2018
BNS WHEAT ROLLS ( Under the following Trade Names - Giant, Harvest Pride, Shoppers and Old Tyme )
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Schmidt Baking Co., Inc.
25 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 7, 2018
Seggiano Artichoke & Garlic Sauce & Spread Net Weight 200g, 7.1 oz, packaged in Glass jar, UPC Code: 812603020381
High riskUsing this product could cause serious injury, illness or death — stop using it now.Seggiano USA Inc.
FDA (openFDA food enforcement)
Reported Mar 7, 2018
ST AIA-PACK¿ PROG II, Progesterone II Assay, Part Number: 025239
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tosoh Bioscience Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 7, 2018
Camera System, Television, Surgical without audio Intended for transmission and documentation of surgical interventions…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trumpf Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Mar 7, 2018
Zimmer Segmental System, ZSS Distal Femur. Sizes as follows: a. Size B-LT (Item No. 00585001201); b. Size B-RT (Item…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 1, 2018
J Bar B Foods Retira Productos De Salchicha De Pollo Debido A Un Error De Rotulacin Y Un Alrgeno No Declarado
High riskUsing this product could cause serious injury, illness or death — stop using it now.J Bar B Foods
USDA FSIS
Reported Feb 28, 2018
Innova Self-Expanding Stent System, 200 mm. Labeled with Material Number and description as follows: Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 28, 2018
Frozen Unbaked Biscuits sold under the brand names of Hilltop Hearth, Mary B's & Marshall.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Holsum Baking Company Warehouse
FDA (openFDA food enforcement)
Reported Feb 28, 2018
IQF Green beans, sold as Not Ready To Eat (NRTE) product for use in foodservice or manufacturing applications. The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.National Frozen Foods Corporation--Seattle
1 more product in this recall
FDA (openFDA food enforcement)
Reported Feb 28, 2018
Pentax Video Duodenoscope Model: ED-3490TK (UDI of design being recalled: 04961333232420) These instruments are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pentax
FDA (openFDA device enforcement)
Reported Feb 28, 2018
Cobas 8000 Modular Series system; Software Version 05-02 and 06-03; UDI: 05641446001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Corporation
FDA (openFDA device enforcement)
Reported Feb 21, 2018
Purely Yours Breast Pump. Model 17070PMW and Model 17070ACA. Intended to express and collect the mother s milk from the…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Ameda, Inc.
FDA (openFDA device enforcement)
Reported Feb 21, 2018
AVID Medical QA Pack AV10654-10
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Avid Medical, Inc.
FDA (openFDA device enforcement)
Reported Feb 21, 2018
BROLITE PRODUCT #6109 BREAD FLAVOR R, Net Wt. 50 Lbs
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brolite Products Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 21, 2018
WALNUT CREEK FOODS Caramel Popcorn NET WT 15 OZ (425g) Ingredients: Evaporated Can Juice, Popcorn, Butter (cream,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Coblentz Distributing Inc. dba Walnut Creek Foods
FDA (openFDA food enforcement)
Reported Feb 21, 2018
Central Venous Catheter Set Triple Lumen Polyurethane, Catalog Identifier: C-UTLM-501J Product Usage: The central…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Virginia recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.