Dark Chocolate Almonds packaged in: 4 oz. Plastic Pouch, 9 oz. Plastic Cup, 9 oz. Stand Up Plastic Pouch, 12 oz. Square Plastic Tub, 17 oz. Family Size Plastic Pouch. Aurora Brand and Store Branded Labeling Include: AG Supermarkets, Belmont Market, Boiceville Market, Decicco s, Graul s 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 - Dangerous
🍎 Food Recalled: November 1, 2017 Aurora Products Snacks & Candy Nationwide

What Should You Do?

  1. Check if you have this product:
    BEST IF USED BY DATE CODE RANGE: 11/01/16 7/30/18
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. 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 Almonds packaged in: 4 oz. Plastic Pouch, 9 oz. Plastic Cup, 9 oz. Stand Up Plastic Pouch, 12 oz. Square Plastic Tub, 17 oz. Family Size Plastic Pouch. Aurora Brand and Store Branded Labeling Include: AG Supermarkets, Belmont Market, Boiceville Market, Decicco s, Graul s 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.gov

FDA Recall Number: F-0338-2018

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