FDA Recall United States Completed Historical recordClass II
Ice Cream Factory, LLC
- Product
- Bakery Graham Pieces, 10 LB Label reads in part as "Ice Crea…
- Published
- November 12, 2025
- Distribution
- Consumers, wholesale and retail location…
Ice Cream Factory, LLC Recall: Foreign material fragments consisting of aluminum foil and packaging material were identified in brown sugar ingredient that may have been used in the products
United States
CompletedClass II
- Company
- Ice Cream Factory, LLC
- Product
- Strawberry Cheesecake Ice Cream with graham crackers swirl,…
- Recall date
- October 23, 2025
- Source
- FDA
Reason for recall
Foreign material fragments consisting of aluminum foil and packaging material were identified in brown sugar ingredient that may have been used in the products
- - Recall initiated
- - Reported by source
| 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 |
Distribution
- Consumers
- wholesale and retail locations in FL
- GA
- NC
- MD
- WI
- WY
- IL
- IA
- IN
- WA
- MO
- AR
- KS
- NE
- LA
- OH
- OK
- PA
- UT
- AL
- TN
- TX
- SD
- SC
- MI
- MN
- MS
- NM and KY
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- H-0166-2026
- Event ID
- 97876
- Status
- Completed
- Classification
- Class II
- Company
- Ice Cream Factory, LLC
- Product description
- 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"
- Quantity
- 979 cases of 12-12oz containers; 313 2.5-gal tubs
- Reason
- Foreign material fragments consisting of aluminum foil and packaging material were identified in brown sugar ingredient that may have been used in the products
- Recall initiation date
- October 23, 2025
- Report date
- November 12, 2025
- Classification date
- Not published in this source record
- Termination date
- Not terminated as of this source record
- Distribution pattern
- Consumers, wholesale and retail locations in FL, GA, NC, MD, WI, WY, IL, IA, IN, WA, MO, AR, KS, NE, LA, OH, OK, PA, UT, AL, TN, TX, SD, SC, MI, MN, MS, NM and KY
- UPC, lot, and code information
- Lot Code/Expiration Date: 25177CF2-1S1C1 06/26/2027 25191CF2-1S1C1 07/10/2027 25231CF4-1S1C1 08/19/2027
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 97876 with 1 other product entry in Public Health Trace.
Responsible company: Ice Cream Factory, LLC
Other recalls from Ice Cream Factory, LLC
FDA Recall United States Completed Historical recordClass II
Ice Cream Factory, LLC
- Product
- Bakery Graham Pieces, 10 LB Label reads in part as "Ice Crea…
- Published
- November 12, 2025
- Distribution
- Consumers, wholesale and retail location…
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.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
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.
Is this recall still active?
According to FDA, this recall's status is "Completed." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
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.
Where can I find more official information?
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.
