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Policy version 2026-07-21, effective July 21, 2026.
United States
TerminatedClass II
Foreign material fragments consisting of aluminum foil and packaging material were identified in brown sugar ingredient that may have been used in the products
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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 Cream Factory 1201 Ice Cream Way, Lebanon, MO 65536" | Not published in this source record | 979 cases of 12-12oz containers; 313 2.5-gal tubs | Lot Code/Expiration Date: 25177CF2-1S1C1 06/26/2027 25191CF2-1S1C1 07/10/2027 25231CF4-1S1C1 08/19/2027 |
This recall shares FDA event ID 97876 with 1 other product entry in Public Health Trace.
FDA Recall United States TerminatedTerminated: August 12, 2026Historical recordClass II
Responsible company: Ice Cream Factory, LLC
FDA Recall United States TerminatedTerminated: August 12, 2026Historical recordClass II
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Florida | 1 |
| Georgia | 1 |
| North Carolina | 1 |
| Maryland | 1 |
| Wisconsin | 1 |
| Wyoming | 1 |
| Illinois | 1 |
| Iowa | 1 |
| Indiana | 1 |
| Washington | 1 |
| Missouri | 1 |
| Arkansas | 1 |
| Kansas | 1 |
| Nebraska | 1 |
| Louisiana | 1 |
| Ohio | 1 |
| Oklahoma | 1 |
| Pennsylvania | 1 |
| Utah | 1 |
| Alabama | 1 |
| Tennessee | 1 |
| Texas | 1 |
| South Dakota | 1 |
| South Carolina | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| Mississippi | 1 |
| New Mexico | 1 |
| Kentucky | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
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