Acidified Tea in a glass bottle with a multi-colored, stick-on label that reads in part: " HARMONY Chai Decaffeinated Fresh brewed on Orcas Island, WA Rooibos Chai 22oz. (624,25ml)***Ingredients: water, Organic Raw Sugar, Rooibos Tea, cloves, cinnamon, Ginger, secret spices, citric Acid***7 94504 02431 9***" There is also a larger size with the same labeling except: "*** 64oz. (1892.70ml)***7 05105 01301 5***"

Class I - Dangerous
Recalled: June 24, 2013 Harmony Chai Beverages

What Should You Do?

  1. Check if you have this product:
    22 oz. Rooibos Chai: 7 94504 02431 9 64 oz. Rooibos Chai: 7 05105 01301 5 The recall involved all lot codes.
  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:
Harmony Chai
Reason for Recall:
Product not properly processed
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Acidified Tea in a glass bottle with a multi-colored, stick-on label that reads in part: " HARMONY Chai Decaffeinated Fresh brewed on Orcas Island, WA Rooibos Chai 22oz. (624,25ml)***Ingredients: water, Organic Raw Sugar, Rooibos Tea, cloves, cinnamon, Ginger, secret spices, citric Acid***7 94504 02431 9***" There is also a larger size with the same labeling except: "*** 64oz. (1892.70ml)***7 05105 01301 5***"

Product Codes/Lot Numbers:

22 oz. Rooibos Chai: 7 94504 02431 9 64 oz. Rooibos Chai: 7 05105 01301 5 The recall involved all lot codes.

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1847-2013

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