Jeni's Passion Fruit Dreamsicle Ice Cream Bars
Recalled by Jeni's Splendid Ice Creams LLC

Class II — moderate
Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
Jeni's Splendid Ice Creams LLC has recalled Jeni's Passion Fruit Dreamsicle Ice Cream Bars, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on December 3, 2025 and was initiated on November 13, 2025. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.
What was recalled?
This recall covers Jeni's Passion Fruit Dreamsicle Ice Cream Bars, with approximately 3,767 cases affected. The company behind the recall is Jeni's Splendid Ice Creams LLC, based in Columbus, OH. The FDA describes the product as: “Jeni's Passion Fruit Dreamsicle Ice Cream Bars, 3 FL OZ (89 ML)/9 FL OZ (266 ML), packaged 3 bars per retail carton with Item UPC: 850060644122, packed 8 retail cartons per case with Case UPC: 10850060644129”
Why was Jeni's Passion Fruit Dreamsicle Ice Cream Bars recalled?
According to the FDA, the stated reason for the recall is: “Undeclared allergens - wheat and soy.” In plain terms, this recall relates to an undeclared ingredient or allergen.
An undeclared ingredient means a food contains something — often a major allergen such as milk, eggs, soy, wheat, peanuts, or tree nuts — that is not listed on the label. For most people this is not dangerous, but for someone with a food allergy or sensitivity it can trigger a serious reaction. Accurate labeling is required so that people can avoid ingredients they need to stay away from.
What should you do?
If you think you may have bought Jeni's Passion Fruit Dreamsicle Ice Cream Bars, compare it against the product description and identifying codes (BEST BY OCT 2026 Packer/Manufacturer Number: 36-3553 Batch/Lot: 25-210 Item Number: 2061) before using it.
The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Jeni's Splendid Ice Creams LLC or your local health authority.
About this recall
This recall was distributed in OH. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.
Full recall details
- Status
- Terminated
- Date reported
- December 3, 2025
- Recall started
- November 13, 2025
- Distributed in
- OH
What you can do
Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.
Quick answers
Why was Jeni's Passion Fruit Dreamsicle Ice Cream Bars recalled?+
According to the FDA: Undeclared allergens - wheat and soy
How serious is this recall?+
Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
What should I do if I have Jeni's Passion Fruit Dreamsicle Ice Cream Bars?+
Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: H-0207-2026. Information last synced from the FDA on July 5, 2026.