Recalled product has the carton labeled as Tillamook 1.5 QT CHOCOLATE PEANUT BUTTER Ice Cream, frozen, 1.5 Qt. and has the correct lid labeled as Tillamook WAFFLE CONE SWIRL ICE...
FINDARECALL QUICK READ
What this record tells you
This FDA record concerns Recalled product has the carton labeled as Tillamook 1.5 QT CHOCOLATE PEANUT BUTTER Ice Cream, frozen, 1.5 Qt. and has the correct lid labeled as Tillamook WAFFLE CONE SWIRL ICE... and names Tillamook County Creamery Association as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.
- Firm: Tillamook County Creamery Association
- Classification: Class II
- Status: Terminated
- Recall date: 2023-05-27
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Product Description & Identification
Recalled product has the carton labeled as Tillamook 1.5 QT CHOCOLATE PEANUT BUTTER Ice Cream, frozen, 1.5 Qt. and has the correct lid labeled as Tillamook WAFFLE CONE SWIRL ICE CREAM. The carton label is read Tillamook CHOCOLATE PEANUT BUTTER ICE CREAM, KEEP FROZEN ***allergen advisory "Made on equipment that makes products containing milk, egg, peanut, soy, tree nuts, wheat *** Distributed by Tillamook County Creamery Association, Tillamook, OR 97141*** UPC 0 72830 08116 0.
Reason for Recall / Hazard Identified
Undeclared Wheat and Soy. Waffle Cone Swirl Ice Cream was mistakenly packaged in Chocolate Peanut Butter cartons with the correct Waffle Cone Swirl lids. Waffle Cone Swirl ice cream contains wheat and soy which are not declared on the Chocolate Peanut Butter label.
How to Check Whether Your Product Matches
A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.
- Confirm the full product and brand or recalling-firm name.
- Compare package size, color, flavor, model, style, or configuration when listed.
- Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
- Review the recall date and distribution information without assuming every seller is listed.
- Open the official FDA source below and follow its current instructions.
If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.
Consumer Action Recorded in the Source
Distribution & Affected States
distributed in ID and WA.
Verify With the Issuing Agency
This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.
Open FDA Source Record →Record Transparency
- Issuing agency
- FDA
- Source ID
- F-0987-2023
- Indexed update
- 2026-08-09 21:59:13 UTC
- Official source
- Open issuing-agency record