Turkeyfoot Creek Creamery Cacao Brownie Bites Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper car
Summary
The FDA issued a Class II for Turkeyfoot Creek Creamery Cacao Brownie Bites Artisan Ice Cream, One Pint (473 m by Turkeyfoot Creek Creamery LLC. Reason: Undeclared allergens - soy and wheat.
Details
Source
Food Recall
External ID
H-0310-2025
Action Date
2025-07-30
Status
Terminated
Category
food
Product Description
Turkeyfoot Creek Creamery Cacao Brownie Bites Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with paper lid
Lot/Code Info: All expiration dates (MM/DD/YY; written on bottom of carton)
Quantity Affected: Unknown
Reason for Recall
Undeclared allergens - soy and wheat
Distribution
Products were distributed to six (6) retailers in: IN, MI, OH
Type: Voluntary: Firm initiated
Recall Initiated: 2025-06-10
Company
Wauseon, OH
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 71 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Turkeyfoot Creek Creamery LLC has 8 FDA actions in our database, including 8 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Turkeyfoot Creek Creamery LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Turkeyfoot Creek Creamery LLC have FDA actions?
Turkeyfoot Creek Creamery LLC has 8 FDA actions in our database, including 8 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0310-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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