Lower riskFood recall · FDA · Published November 13, 2025
Jeni's Passion Fruit Dreamsicle Ice Cream Bars Recall: Undeclared Wheat and Soy Allergens
Jeni's recalls Passion Fruit Dreamsicle Ice Cream Bars due to undeclared wheat and soy allergens. Consumers should check packaging for UPC 850060644122 to determine if affected.
“Jeni's Passion Fruit Dreamsicle Ice Cream Bars Recall: Undeclared Wheat and Soy Allergens.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/6978-jeni-s-passion-fruit-dreamsicle-ice-cream-bars-recall-undeclared. Based on FDA recall #H-0207-2026.
The FDA announced on Nov. 13, 2025, that Jeni's Splendid Ice Creams LLC is recalling Passion Fruit Dreamsicle Ice Cream Bars due to undeclared wheat and soy allergens. Consumers should check their product labels for the specific UPCs and lot codes listed in this notice.
How to tell if you have it
Jeni's Passion Fruit Dreamsicle Ice Cream Bars, 3 FL OZ (89 ML)/9 FL OZ (266 ML)
UPC: 00850060644122
Case UPC: 10850060644129
Best By: OCT 2026
Packer/Manufacturer Number: 36-3553
Batch/Lot: 25-210
Item Number: 2061
The hazard
The ice cream bars contain undeclared wheat and soy allergens, which pose a risk to individuals with allergies to these ingredients. The FDA classified the recall as Class II.
Context
GovInfoNow's records show Jeni's Splendid Ice Creams LLC has issued three other recalls since April 22, 2015. Other recent recalls of similar products include Loard's Almond Joy Ice Cream Recall (April 15, 2026), Silver Moon Chocolate Showers Ice Cream Recall (April 15, 2026), and Loard's Horchata Ice Cream Recall (April 15, 2026).
How to tell if you have this one
Check for the UPC 850060644122 on the product packaging. The product was packaged in retail cartons of 3 bars per carton, with a best by date of October 2026.
Brand
Jeni's
Product
Jeni's Passion Fruit Dreamsicle Ice Cream Bars, 3 FL OZ (89 ML)/9 FL OZ (266 ML), packaged 3 bars per retail carton
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Packaging
Look for the UPC 850060644122 on the product packaging to confirm if it's affected.
Where it went and when
Where it was distributed
Distributed in 10 states.
Listed by the agency
Not listed
FDA distribution: “CA, FL, GA, IA, IL, NC, NH, NY, TX, WA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Florida, Georgia, Illinois, Iowa, New Hampshire, New York, North Carolina, Texas, Washington.
Recall timeline
FDA terminated this recall 4 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #H-0207-2026 (November 13, 2025)
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.