Huckleberry Chip ice cream, labeled in part, "***Full Tilt ice cream Huckleberry Chip***Ingredients: Cream, milk, sugar, skim milk powder...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (listeria). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1052-2015.
Full Tilt Brand ice cream is being recalled due to the potential to be contaminated with Listeria monocytogenes. These products contain ice cream mix, an ingredient manufactured and recalled by Snoqualmie Gourmet Ice Cream, Inc.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1052-2015.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Full Tilt Ice Cream or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1052-2015.
Full Tilt Ice Cream
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
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If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Full Tilt Ice Cream Recall FAQ
Full Tilt Ice Cream is the subject of a dairy safety report: Huckleberry Chip ice cream, labeled in part, "***Full Tilt ice cream Huckleberry Chip***Ingredients: Cream, milk, sugar, skim milk powder.... The notice was published on December 22, 2014 by the U.S. Food and Drug Administration (FDA). Approximately 394 units are potentially affected.