Dark Chocolate Cranberries packaged in: Bulk 3.5 oz. Plastic Cup 4.75 oz. Plastic Pouch 9 oz. Plastic Cup 9 oz. Plastic Pouch 11 oz. Square Plastic Tub 18 oz. Family Size Plastic Pouch 26 oz. Plastic Tray Aurora Brand and Store Branded Labeling Include: AG Supermarkets, Belmont Market, Boiceville Market, Deciccos, Grauls Market, Gourmet Garage, Harvest Co Op Market, Hurley Ridge, Lees Supermarket, Morton Williams, Palmers Market, Walter Stewart, Windfall Market and Whole Food Market.
Class I - DangerousWhat Should You Do?
- Check if you have this product: BEST IF USED BY DATE CODE RANGE: 11/01/16 7/30/18
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Aurora Products, Inc.
- Reason for Recall:
- Product contains undeclared milk
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Dark Chocolate Cranberries packaged in: Bulk 3.5 oz. Plastic Cup 4.75 oz. Plastic Pouch 9 oz. Plastic Cup 9 oz. Plastic Pouch 11 oz. Square Plastic Tub 18 oz. Family Size Plastic Pouch 26 oz. Plastic Tray Aurora Brand and Store Branded Labeling Include: AG Supermarkets, Belmont Market, Boiceville Market, Deciccos, Grauls Market, Gourmet Garage, Harvest Co Op Market, Hurley Ridge, Lees Supermarket, Morton Williams, Palmers Market, Walter Stewart, Windfall Market and Whole Food Market.
Product Codes/Lot Numbers:
BEST IF USED BY DATE CODE RANGE: 11/01/16 7/30/18
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-0340-2018
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