Recall Register

Food, drugs, devices

Food recall: Turkeyfoot Creek Creamery Avalanche Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with p

FDA enforcement event 97071 · Class II · initiated 10 Jun 2025 · status Terminated · terminated 12 Sep 2025

FoodVoluntary: Firm initiated8 product recordsWauseon, OH

FDA enforcement event 97071 is a food recall by Turkeyfoot Creek Creamery LLC of Wauseon, OH, initiated 10 Jun 2025 and classified Class II, with 8 product records.

FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 54% of the 569 food enforcement events initiated in 2025 carry the same class.

Status: Terminated, terminated 12 Sep 2025. Initiation: voluntary: firm initiated. This is the only enforcement event on this register for Turkeyfoot Creek Creamery LLC.

Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.

Recalling firm

Turkeyfoot Creek Creamery LLC, Wauseon, OH.

Reason for recall

"Undeclared allergens - soy and wheat"

Distribution

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

Product records

Recall numberProductQuantityClassStatusReport date
H-0308-2025Turkeyfoot Creek Creamery Avalanche Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with paper lidUnknownClass IITerminated30 Jul 2025
H-0309-2025Turkeyfoot Creek Creamery Chocolate Peanut Butter Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with paper lidUnknownClass IITerminated30 Jul 2025
H-0310-2025Turkeyfoot Creek Creamery Cacao Brownie Bites Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with paper lidUnknownClass IITerminated30 Jul 2025
H-0311-2025Turkeyfoot Creek Creamery Cookies and Cream Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with paper lidUnknownClass IITerminated30 Jul 2025
H-0312-2025Turkeyfoot Creek Creamery Cookie Dough Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with paper lidUnknownClass IITerminated30 Jul 2025
H-0313-2025Turkeyfoot Creek Creamery Cacao Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with paper lidUnknownClass IITerminated30 Jul 2025
H-0314-2025Turkeyfoot Creek Creamery Mocha Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with paper lidUnknownClass IITerminated30 Jul 2025
H-0315-2025Turkeyfoot Creek Creamery Cacao Strawberry Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with paper lidUnknownClass IITerminated30 Jul 2025

Context

54%of 2025 food events are Class II569 events that year
8product records in this event
1event on this register for the firm

Questions and answers

Why was this food recalled?

FDA's record gives the reason for recall as: "Undeclared allergens - soy and wheat"

What does Class II mean?

FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.

Where was the product distributed?

FDA's distribution pattern field reads: "Products were distributed to six (6) retailers in: IN, MI, OH"

Is the recall still ongoing?

FDA lists the status as Terminated; the termination date is 12 Sep 2025. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.

Where does this data come from?

openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.

Provenance

Source: openFDA food enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.