🔍 RecallPedia

Pow Pow Powders: A standard of Quality Hot Cocoa Mix; NET Wt. 3.50 lb. (1.59kg) Ingredients: Sugar, Non-Dairy Creamer (coconut oil, Corn Syrup Solids, Sodium Caseinate (a milk derivative), Sodium Citrate, Mono and Diglycerides, Salt), Cocoa (processed with alkali) Non-Fat Dry Milk, Corn Syrup Solids, Salt, Natural and Artificial flavor, Silicon Dioxide (to prevent caking agent) and Carrageenan.

Class I - Dangerous
Recalled: June 29, 2021 San Diego Coffee, Tea and Spice Dairy & Eggs

What Should You Do?

  1. Check if you have this product:
    90265/2141552
  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:
San Diego Coffee, Tea and Spice
Reason for Recall:
FDA inspection found that various smoothie mixes sold to restaurants did not include ingredient list or allergen information (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:

Pow Pow Powders: A standard of Quality Hot Cocoa Mix; NET Wt. 3.50 lb. (1.59kg) Ingredients: Sugar, Non-Dairy Creamer (coconut oil, Corn Syrup Solids, Sodium Caseinate (a milk derivative), Sodium Citrate, Mono and Diglycerides, Salt), Cocoa (processed with alkali) Non-Fat Dry Milk, Corn Syrup Solids, Salt, Natural and Artificial flavor, Silicon Dioxide (to prevent caking agent) and Carrageenan.

Product Codes/Lot Numbers:

90265/2141552

Distribution:

Distributed in: CA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0785-2021

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