سحب منتجات Turkeyfoot Creek Creamery بسبب مسبب حساسية غير معلن

United States

Update July 21st, 2025:
The FDA has updated the reason for recall wording for the affected Turkeyfoot Creek Creamery ice cream products. While the underlying issue remains the same (undeclared soy and wheat allergens), the phrasing in the official recall notice has been revised for clarity. The reason for the recall for all eight products has been updated as follows:

PREVIOUS WORDING
- Undeclared allergens (soy and wheat) in the "Contains" statement
- Undeclared allergen (soy) in the "Contains" statement

NEW WORDING:
- Undeclared allergens - soy and wheat
- Undeclared allergen - soy

No changes were made to the affected products, distribution areas, or packaging. The updated wording clarifies the presence of undeclared allergens in these products, which can pose a risk to those with soy and/or wheat allergies.

Consumers who are allergic or sensitive to soy or wheat should not consume these products. If you have already consumed any of the recalled ice cream and have experienced symptoms, please seek medical advice.

Source: Access Data FDA


July 20th, 2025:
Turkeyfoot Creek Creamery LLC has issued a voluntary recall of several ice cream products due to undeclared allergens, specifically soy and wheat. The products were distributed to six retailers in Indiana, Michigan, and Ohio in the United States.

AFFECTED PRODUCTS:
1) PRODUCT: Turkeyfoot Creek Creamery Avalanche Artisan Ice Cream, One Pint (473 ml)
- Packaged individually in a paper carton with paper lid
- Code Information: All expiration dates (MM/DD/YY; written on bottom of carton)
- Undeclared allergens (soy and wheat) in the "Contains" statement

2) PRODUCT: Turkeyfoot Creek Creamery Chocolate Peanut Butter Artisan Ice Cream, One Pint (473 ml),
- Packaged individually in a paper carton with paper lid
- Code Information: All expiration dates (MM/DD/YY; written on bottom of carton)
- Undeclared allergen (soy) in the "Contains" statement

3) PRODUCT: Turkeyfoot Creek Creamery Cacao Brownie Bites Artisan Ice Cream, One Pint (473 ml)
- Packaged individually in a paper carton with paper lid
- Code Information: All expiration dates (MM/DD/YY; written on bottom of carton)
- Undeclared allergens (soy and wheat) in the "Contains" statement

4) PRODUCT: Turkeyfoot Creek Creamery Cookies and Cream Artisan Ice Cream, One Pint (473 ml)
- Packaged individually in a paper carton with paper lid
- Code Information: All expiration dates (MM/DD/YY; written on bottom of carton)
- Undeclared allergens (soy and wheat) in the "Contains" statement

5) PRODUCT: Turkeyfoot Creek Creamery Cookie Dough Artisan Ice Cream, One Pint (473 ml)
- Packaged individually in a paper carton with paper lid
- Code Information: All expiration dates (MM/DD/YY; written on bottom of carton)
- Undeclared allergens (soy and wheat) in the "Contains" statement

6) PRODUCT: Turkeyfoot Creek Creamery Cacao Artisan Ice Cream, One Pint (473 ml)
- Packaged individually in a paper carton with paper lid
- Code Information: All expiration dates (MM/DD/YY; written on bottom of carton)
- Undeclared allergen (soy) in the "Contains" statement

7) PRODUCT: Turkeyfoot Creek Creamery Mocha Artisan Ice Cream, One Pint (473 ml)
- Packaged individually in a paper carton with paper lid
- Code Information: All expiration dates (MM/DD/YY; written on bottom of carton)
- Undeclared allergen (soy) in the "Contains" statement

8) PRODUCT: Turkeyfoot Creek Creamery Cacao Strawberry Artisan Ice Cream, One Pint (473 ml)
- Packaged individually in a paper carton with paper lid
- Code Information: All expiration dates (MM/DD/YY; written on bottom of carton)
- Undeclared allergen (soy) in the "Contains" statement

The recall includes all expiration dates of the following one-pint ice cream varieties: Avalanche, Chocolate Peanut Butter, Cacao Brownie Bites, Cookies and Cream, Cookie Dough, Cacao, Mocha, and Cacao Strawberry. Each product is packaged in a paper carton with a paper lid. The exact quantity of products recalled is unknown.

The issue was discovered through a notification process. The recall, classified as Class II, was initiated on June 10, 2025, and classified on July 18, 2025.



Source: www.accessdata.fda.gov/scripts/ires/index.cfm