Recchiuti Bittersweet, Smooth, rich and complex. Net Wt. 3 oz. (85 G) Also sold in case of 12 UPC 8019895 00017 6 Ingredient: Dark chocolate {cocoa beans, sugar, cocoa butter, soy lecithin (emulsifier)} Natural vanilla extract, cacao paste. Contains: soy Made on equipment also shared with soy, milk, wheat, eggs, peanuts and tree nuts. Manufactured by Recchiuti Confections, San Francisco, CA

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Lot code 21418000 (Best Buy 7/2/19) Lot code 16518000 (Best Buy 5/14/19)
  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:
Confections by Michael Recchiuti
Reason for Recall:
FDA analysis of Dairy Free Dark Chocolate found high levels of milk protein in the chocolate bars.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Recchiuti Bittersweet, Smooth, rich and complex. Net Wt. 3 oz. (85 G) Also sold in case of 12 UPC 8019895 00017 6 Ingredient: Dark chocolate {cocoa beans, sugar, cocoa butter, soy lecithin (emulsifier)} Natural vanilla extract, cacao paste. Contains: soy Made on equipment also shared with soy, milk, wheat, eggs, peanuts and tree nuts. Manufactured by Recchiuti Confections, San Francisco, CA

Product Codes/Lot Numbers:

Lot code 21418000 (Best Buy 7/2/19) Lot code 16518000 (Best Buy 5/14/19)

Distribution:

Distributed in: CA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0698-2019

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