Heart of the Earth (HOTE) 100% Pure Ceremonial Cacao Pre-Ground Paste. Net Wt. 16oz (454g). Packaged in Kraft paper heat sealed stand-up pouch bags with inner plastic liner with SKU PC-GRUCCP-1LB. Product of Guatemala. Distributed Soul Lift Cacao of Portland, Oregon. The product is 100% pure cacao (chocolate) which is not ready for consumption. In most cases it is prepared into a chocolate drink with hot water and a blender.

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Lot #506 with "best by" date June 18, 2026.
  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:
Inner Waymark LLC
Reason for Recall:
Elevated lead level 0.671 ppm in cacao (chocolate)
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Heart of the Earth (HOTE) 100% Pure Ceremonial Cacao Pre-Ground Paste. Net Wt. 16oz (454g). Packaged in Kraft paper heat sealed stand-up pouch bags with inner plastic liner with SKU PC-GRUCCP-1LB. Product of Guatemala. Distributed Soul Lift Cacao of Portland, Oregon. The product is 100% pure cacao (chocolate) which is not ready for consumption. In most cases it is prepared into a chocolate drink with hot water and a blender.

Product Codes/Lot Numbers:

Lot #506 with "best by" date June 18, 2026.

Distribution:

Distributed in: CA, FL, IL, KY, MD, ME, MI, MO, MT, NH, NY, OR, TX, UT, WI

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0004-2025