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Jivara Lactee Milk Chocolate Valrhona; 40% Ingredients: Cocoa Butter, whole powdered milk, sugar, cocoa beans, brown sugar, natural vanilla extract, soya lecithin, malt extract, Natural Vanilla Flavor. Contains: Soy,. May contain trace amounts of dairy, eggs, nuts and gluten as it produced on the same machinery. UPC 2503044025508 Whole Foods Market, Emeryville, CA 95408

Class I - Dangerous
Recalled: May 23, 2015 Whole Foods Market Dairy & Eggs

What Should You Do?

  1. Check if you have this product:
    Pac dates prior to May 19, 2915. UPC 2503044025508.
  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:
Whole Foods Market
Reason for Recall:
One retail location incorrectly labeled Jivara Lactee Milk Chocolate Valrhona cut and wrap pieces without hazelnuts declared on the product label.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Jivara Lactee Milk Chocolate Valrhona; 40% Ingredients: Cocoa Butter, whole powdered milk, sugar, cocoa beans, brown sugar, natural vanilla extract, soya lecithin, malt extract, Natural Vanilla Flavor. Contains: Soy,. May contain trace amounts of dairy, eggs, nuts and gluten as it produced on the same machinery. UPC 2503044025508 Whole Foods Market, Emeryville, CA 95408

Product Codes/Lot Numbers:

Pac dates prior to May 19, 2915. UPC 2503044025508.

Distribution:

Distributed in: CA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-2738-2015

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