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 48,122 notices were distributed nationwide, so they reach Virginia too — those are in the archive.

Medical devices

Reported Nov 13, 2019

Babi.Plus 12.5 cm H2O Pressure Relief Manifold Catalog # 2691 for use with ventilators.

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

Teleflex-Morrisville

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2019

BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608

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

Becton Dickinson & Company

FDA (openFDA device enforcement)

Food

Reported Nov 6, 2019

Blue Bell Butter Crunch Ice Cream packaged in a 1/2 Gallon (2 Qts) paperboard cup & lid (4 units per corrugated sleeve,…

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

Blue Bell Creameries, LP

FDA (openFDA food enforcement)

Medical devices

Reported Nov 6, 2019

Implant Direct Scan Adapter Assembly Replant platform for the following part numbers: 6035-09PT-M (3.5mmD)/UDI :…

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

Implant Direct Sybron Manufacturing, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2019

C3 Wave App, v. 2.0.5

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

Medical Components, Inc. dba MedComp

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2019

Model No. 01-1501-0032 (Child Nail Attachment Bolt). Component of the Pediatric Nailing Platform. Product Usage: an…

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

OrthoPediatrics Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 6, 2019

Bulk Dry Apricot in clear plastic bags inside brown cardboard box and Swan brand Dry Appricot & Keshav brand Dry…

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

Peekay International, Inc.

FDA (openFDA food enforcement)

Food

Reported Nov 6, 2019

GANCHI NAIWEITANGPIAN Candy NET WT: 280G(9.8oz) in cardboard package. 24 packages per master case. The following codes…

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

Rong Shing Trading Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 6, 2019

Synchro2, 0.014 in x 200cm, SOFT Guidewire with Hydrophilic Coating, UPN Product No. M00326010 REF 2601, STERILE: EO -…

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

Stryker Neurovascular

7 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 6, 2019

Jack Daniels Tennessee Whiskey Cake - Chocolate - Net Wt 8 OZ (227 g), UPC: 854621004349

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

The Great Spirits Baking Company, LLC

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 6, 2019

Posey Connected Twice-As-Tough Cuffs

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

Tidi Products

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

Sterile Co-Flex NL 3" - Product Usage: Single Use secondary wound dressing or compression wrap.

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

Andover Healthcare Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

EXACTAMIX Empty EVA (Ethylene Vinyl Acetate) TPN Bag with the following product code and sizes: 1. H938737, 250mL; 2.…

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

Canister HFC-134a /1000g, ALUM Product Number: 1600-00-0218 Revision .0C Coolant canister for use with surgical laser.

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

Candela Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 30, 2019

Dole Crushed Pineapple in 100% pineapple juice Manufactured For Dole Packaged Foods, LLC Westlake Village, CA 91361…

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

Dole Packaged Foods, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Oct 30, 2019

Ergo 3.2mm K-wire - Product Usage: The devices is used assist the surgeon in the implantation of Equinoxe Shoulder…

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

Exactech, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

ApexPro Telemetry Server System. Also identified as Modification To: ApexPro Telemetry System and ApexPro FH Telemetry…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

The ICS CHARTR EP 200

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

GN Otometrics

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

Irrisept Wound Debridement and Cleansing System. 12 units per case.

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

IrriMAX Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

Torrent Suite Dx Software Version (IUO) 5.2 Catalog Number: A29225 OEM Customer Software: Sentosa SQ Suite Software…

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

Life Technologies Holdings Pte Ltd.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 30, 2019

Premo and Fresh Grab Chicken Salad wheat sandwiches, 5 oz., with UPC code 612510002032.

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

Lipari Foods Operating Company, LLC.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 30, 2019

Semi-Rigid Suction Canister, 3000cc. Model Numbers OR530 and OR530H. For OR530, the product comes in a case with two…

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

Medline Industries Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 30, 2019

Tuna salad under the following brand names: BALLARDS FARM Barboursville, WV 25504 UPC 076010000293 12 oz. plastic…

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

Mrs. Stratton's Salads, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 30, 2019

GRIPPER Needles sold individually. Labeled as the following item descriptions: 1. NDL, GRIPPER, 22G X 1" (25MM), 12/BX;…

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

Smiths Medical ASD Inc.

1 more product in this recall

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.