Cream (Bulk; approximately 40,000 pounds per tanker load)

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    The Dannon Company: Batch No.'s 1002810163 1002810445 1002810700 1002810745 1002810885 1002811154 1002811681 1002811849 1002811932 Dean Foods: Batch No. 1002812313 Unilever: Batch No. 1002810249 Continental Dairy Facilities, LLC: Load No. 990000000000055717
  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:
Dairy Farmers of America
Reason for Recall:
Two loads of raw milk shipped from Beaver Creek Farm located in Coopersville, MI tested positive for Supra Sulfa III (Sulfamethazine). One load was co-mingled with other loads of raw milk at the DFA facility in Adrian, MI and processed into cream and condensed skim milk. The second load went directly from the producers farm to Continental Dairy Facilities, LLC in Coopersville, Michigan and was fur
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Cream (Bulk; approximately 40,000 pounds per tanker load)

Product Codes/Lot Numbers:

The Dannon Company: Batch No.'s 1002810163 1002810445 1002810700 1002810745 1002810885 1002811154 1002811681 1002811849 1002811932 Dean Foods: Batch No. 1002812313 Unilever: Batch No. 1002810249 Continental Dairy Facilities, LLC: Load No. 990000000000055717

Distribution:

Distributed in: OH, IL, MO, MI

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-2486-2014

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