🔍 RecallPedia

CCF Butter Popcorn Seasoning, NET Wt. 1000 lbs, Gluten Free

Class I - Dangerous
Recalled: December 7, 2016 Dutch-American Foods Dairy & Eggs

What Should You Do?

  1. Check if you have this product:
    Lot#: 61101DA251, 61101DA252, 61101DA253, 61101DA254, 61101DA255, 61101DA256, 61101DA257, 61128DA201, 61128DA202, 61128DA203, 61128DA204, 61128DA205, 61128DA206, 61128DA207, 60627DA201, 60627DA202, 60627DA203, 60627DA204, 60627DA205, 60627DA206, 60627DA207, 60802DA168, 60802DA169, 60802DA170, 60802DA171, 60802DA172, 60802DA173, 60802DA174, 60908DA201, 60908DA202, 60908DA203, 60908DA204, 60908DA205, 60908DA206, 60908DA207, 60922DA201, 60922DA202, 60922DA203, 60922DA204, 60922DA205, 60922DA206, 60922DA207
  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:
Dutch-American Foods Inc
Reason for Recall:
Dutch-American foods is recalling various seasoning products and baking bases due to potential contamination of product with Salmonella.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

CCF Butter Popcorn Seasoning, NET Wt. 1000 lbs, Gluten Free

Product Codes/Lot Numbers:

Lot#: 61101DA251, 61101DA252, 61101DA253, 61101DA254, 61101DA255, 61101DA256, 61101DA257, 61128DA201, 61128DA202, 61128DA203, 61128DA204, 61128DA205, 61128DA206, 61128DA207, 60627DA201, 60627DA202, 60627DA203, 60627DA204, 60627DA205, 60627DA206, 60627DA207, 60802DA168, 60802DA169, 60802DA170, 60802DA171, 60802DA172, 60802DA173, 60802DA174, 60908DA201, 60908DA202, 60908DA203, 60908DA204, 60908DA205, 60908DA206, 60908DA207, 60922DA201, 60922DA202, 60922DA203, 60922DA204, 60922DA205, 60922DA206, 60922DA207

Distribution:

Distributed in: MD, MI, IL, FL

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1301-2017

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