Jump Dark Teriyaki Sauce .5 gallon plastic bag Ingredients: WATER, SUGAR, SOY SAUCE***ALL PURPOSE FLOUR WHITE BLEACHED ENRICHED***DRIED YEAST. Contains: (Soy, Wheat) FOR INSTITUTIONAL USE ONLY Prepared for Jump International HIllard, Ohio 43026 UPC 8 56460 00114 5

Class I - Dangerous
Recalled: June 14, 2016 Sunrise Foods Beverages

What Should You Do?

  1. Check if you have this product:
    J14-2019-2, Item # 36-1875 Lot Dates 1/8/2016, 1/15/2016, 1/18/2016, 1/22/2016, 1/26/2016, 2/1/2016, 2/8/2016, 2/29/2016, 3/30/2016, 4/7/2016, 4/11/2016, 4/27/2016, 5/5/2016
  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:
Sunrise Foods Inc
Reason for Recall:
The firm was notified by their supplier that the flour used in their products may be contaminated with E. Coli.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Jump Dark Teriyaki Sauce .5 gallon plastic bag Ingredients: WATER, SUGAR, SOY SAUCE***ALL PURPOSE FLOUR WHITE BLEACHED ENRICHED***DRIED YEAST. Contains: (Soy, Wheat) FOR INSTITUTIONAL USE ONLY Prepared for Jump International HIllard, Ohio 43026 UPC 8 56460 00114 5

Product Codes/Lot Numbers:

J14-2019-2, Item # 36-1875 Lot Dates 1/8/2016, 1/15/2016, 1/18/2016, 1/22/2016, 1/26/2016, 2/1/2016, 2/8/2016, 2/29/2016, 3/30/2016, 4/7/2016, 4/11/2016, 4/27/2016, 5/5/2016

Distribution:

Distributed in: AL, AR, AZ, CA, CO, IL, IN, KY, MI, MN, MS, NJ, NY, OH, PA, VA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-2205-2016

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