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:
- Return it to the store where you bought it, or throw it away.
- 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.
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
- Weekly archive
- Listed the week of Oct 26, 2026
- 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
- Hazard
- Sterility problem
- 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.
Sunny Sky Products began the recall
FDA posted the recall to its Enforcement Report and rated it Class II (moderate risk)
Added to Recall Canary
Summary updated

