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FDA recall, , Moderate risk

Sunny Sky Non-Dairy French Vanilla Creamer

Sunny Sky Non-Dairy French Vanilla Creamer may have compromised sterility.

What happened

Sunny Sky Products, LLC, of Douglassville, Pennsylvania, voluntarily recalled 1876 cases of Sunny Sky Non-Dairy French Vanilla Creamer, 96oz, bag in box, 3 per case, refrigerate after opening, on September 2, 2026, because the product sterility was potentially compromised. The FDA added the recall to its Enforcement Report and classified it on October 28, 2026.

The product was distributed to Arkansas, California, Georgia, Kentucky, Minnesota, North Carolina, New Mexico, Nevada, Ohio, Texas and Utah.

What to do

The FDA notice gives no instructions for this recall. FDA's general advice for food recalls:

  1. Return it to the store where you bought it, or throw it away.
  2. Don't give it to anyone else, such as a food bank, or to a pet.

Is yours affected?

Affected if its lot code matches.

  1. Sunny Sky Non-Dairy French Vanilla Creamer, 96oz , bag in box, 3 per case, refrigerate after opening

    Lot code
    • L0437F083101

Recall details

Posted by FDA
Recall began
Status
Open
Sold in

The adulterated product was distributed to the following States: Georgia, Texas, Utah, Minnesota, New Mexico, Ohio, North Carolina, California, Kentucky, Arkansas, Nevada,

Recalled by
Sunny Sky Products, LLCDouglassville, Pennsylvania
Risk

Moderate risk

Eating it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.

FDA Class II recall · How risk is rated

FDA event number
99881
Recall number
H-0182-2027
Quantity recalled
1876 Cases
Recall type
Voluntary: Firm initiated
How the company first told customers
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

All recalls from Sunny Sky Products, LLC

Timeline

FDA's Enforcement Report is its public list of recalls; FDA posts a recall by adding it there.

  1. Sunny Sky Products began the recall

  2. FDA posted the recall to its Enforcement Report and rated it Class II (moderate risk)

  3. Added to Recall Canary

  4. Summary updated

Summary by Recall Canary, written with AI · summary updated Oct 31, 2026 · primary source: U.S. Food and Drug Administration (opens in a new tab)