Strawberry Cheesecake Ice Cream with graham crackers swirl
Recalled by Ice Cream Factory, LLC
Food recall
Ice Cream Factory, LLC
Class II — moderate
Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
Ice Cream Factory, LLC has recalled Strawberry Cheesecake Ice Cream with graham crackers swirl, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on November 12, 2025 and was initiated on October 23, 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 Strawberry Cheesecake Ice Cream with graham crackers swirl, with approximately 979 cases of 12-12oz containers; 313 2.5-gal tubs affected. The company behind the recall is Ice Cream Factory, LLC, based in Lebanon, MO. The FDA describes the product as: “Strawberry Cheesecake Ice Cream with graham crackers swirl, 12 oz pack, Single Cup Net Wt: 8.75oz, Case of 12 Strawberry Cheesecake with graham cracker swirl, 2.5-gal Tub, Net Weight 14 pounds Labels read in part as "Ice Cream Factory, Distributed by Ice Crea…”
Why was Strawberry Cheesecake Ice Cream with graham crackers swirl recalled?
According to the FDA, the stated reason for the recall is: “Foreign material fragments consisting of aluminum foil and packaging material were identified in brown sugar ingredient that may have been used in the products.” In plain terms, this recall relates to foreign material.
A foreign material recall means that pieces of something which should not be in food — such as metal, plastic, or glass — may be present. These can pose a choking hazard or cause injury. Recalls like these are issued to remove the affected product before anyone is hurt.
What should you do?
If you think you may have bought Strawberry Cheesecake Ice Cream with graham crackers swirl, compare it against the product description and identifying codes (Lot Code/Expiration Date: 25177CF2-1S1C1 06/26/2027 25191CF2-1S1C1 07/10/2027 25231CF4-1S1C1 08/19/2027) 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 Ice Cream Factory, LLC or your local health authority.
About this recall
This recall was distributed in MO. 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
- Completed
- Date reported
- November 12, 2025
- Recall started
- October 23, 2025
- Distributed in
- MO
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 Strawberry Cheesecake Ice Cream with graham crackers swirl recalled?+
According to the FDA: Foreign material fragments consisting of aluminum foil and packaging material were identified in…
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 Strawberry Cheesecake Ice Cream with graham crackers swirl?+
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-0166-2026. Information last synced from the FDA on July 6, 2026.