Strawberry Cheesecake Ice Cream with graham crackers swirl, 12 oz pack, Single Cup Net Wt: 8.75oz, Case of 12 Strawberr
Summary
The FDA issued a Class II for Strawberry Cheesecake Ice Cream with graham crackers swirl, 12 oz pack, Single C by Ice Cream Factory, LLC. Reason: Foreign material fragments consisting of aluminum foil and packaging material were identified in brown sugar ingredient that may have been used in the.
Details
Source
Food Recall
External ID
H-0166-2026
Action Date
2025-11-12
Status
Completed
Category
food
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"
Lot/Code Info: Lot Code/Expiration Date: 25177CF2-1S1C1 06/26/2027 25191CF2-1S1C1 07/10/2027 25231CF4-1S1C1 08/19/2027
Quantity Affected: 979 cases of 12-12oz containers; 313 2.5-gal tubs
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
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
Type: Voluntary: Firm initiated
Recall Initiated: 2025-10-23
Company
Lebanon, MO
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 34 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Ice Cream Factory, LLC has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Ice Cream Factory, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Ice Cream Factory, LLC have FDA actions?
Ice Cream Factory, LLC has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0166-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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