Lipton Pure Leaf Iced Tea Unsweetened 18.5OZ PL 6 Pack and 12 Pack

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Item # 133244 (6 pk) and Item # 134072 (12 pk) with codes: XXXXGG03034, XXXXGG03044, and XXXXGG03054. Manufactured on: 03/03/14, 03/04/14, and 03/05/14. BTL: Oct 06 14 Code Interpretation as follows: OCT 06 14 XXXXGG03034 Where: OCT 06 14 = End Date XXXX= Military Time (0000-2359) GG = Plt. Designator 03034= Prod Date (03/03/14)
  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:
Pepsi Beverages Company
Reason for Recall:
Pepsi Co has announced a recall of some Lipton Pure Leaf Iced Tea products produced on March 3, 4, 5, and 6th of 2014 due to recent consumer complaints regarding apparent mold in the product.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Lipton Pure Leaf Iced Tea Unsweetened 18.5OZ PL 6 Pack and 12 Pack

Product Codes/Lot Numbers:

Item # 133244 (6 pk) and Item # 134072 (12 pk) with codes: XXXXGG03034, XXXXGG03044, and XXXXGG03054. Manufactured on: 03/03/14, 03/04/14, and 03/05/14. BTL: Oct 06 14 Code Interpretation as follows: OCT 06 14 XXXXGG03034 Where: OCT 06 14 = End Date XXXX= Military Time (0000-2359) GG = Plt. Designator 03034= Prod Date (03/03/14)

Distribution:

Distributed in: DE, IA, IL, KY, MD, MN, MO, NJ, NY, OH, PA, SD, TN, VA, WI

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1962-2014

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