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FDA source record Class II Terminated

Turkeyfoot Creek Creamery Cookie Dough Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with paper lid

Recall Date: 2025-06-10 Recalling Firm: Turkeyfoot Creek Creamery LLC Record Ref: H-0312-2025

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns Turkeyfoot Creek Creamery Cookie Dough Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with paper lid and names Turkeyfoot Creek Creamery LLC 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: Turkeyfoot Creek Creamery LLC
  • Classification: Class II
  • Status: Terminated
  • Recall date: 2025-06-10
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Product Description & Identification

Turkeyfoot Creek Creamery Cookie Dough Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with paper lid

Reason for Recall / Hazard Identified

Undeclared allergens - soy and wheat

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.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. 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

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Distribution & Affected States

Products were distributed to six (6) retailers in: IN, MI, OH

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.

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Record Transparency

Issuing agency
FDA
Source ID
H-0312-2025
Indexed update
2026-08-09 21:59:13 UTC
Official source
Open issuing-agency record