The Doctor's Cure Ice Cream Recalled for Missing Allergen Labels
Koogee-Queen Anne, LLC is recalling The Doctor's Cure Ice Cream because bulk product lacked labels declaring direct allergens and facility processing information.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves allergen mislabeling on common allergens (peanuts, tree nuts, wheat, milk, eggs), which corresponds to a severity score of 3 (High) per the rubric.
Plain-English summary
Koogee-Queen Anne, LLC, d/b/a The Comfy Cow, is recalling 5.2 quarts of The Doctor's Cure Ice Cream. The product was distributed in the states of Indiana and Kentucky. The recall involves specific units identified by codes 1aTDC030314, 1bTDC030314, 1dTDC030314, 1bTDC033114, and 1dTDC021914.
The recall was initiated after an FDA inspection revealed that the bulk product lacked labels. Due to the absence of an ingredient statement, the firm failed to declare direct allergens. Additionally, the products lacked the required declaration that they are packaged in a facility that processes peanuts, tree nuts, wheat, milk, and eggs.
Consumers who purchased this product should check their labels for the specific codes listed above. If the product matches the description and codes, consumers should stop using it and contact the manufacturer for further instructions.
The recalled product
- Product
- The Doctor's Cure Ice Cream. Manufactured by: Koogee-Queen Anne, LLC, d/b/a The Comfy Cow 2221 Frankfort Ave, Louisville, KY 40206.
- Manufacturer
- Koogee-Queen Anne, LLC
- Category
- Food — Ice Cream
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (5)
- 1aTDC030314
- 1bTDC030314
- 1dTDC030314
- 1bTDC033114
- and 1dTDC021914.
Distribution
Part of a larger recall action
This product is one of 78 recalled by Koogee-Queen Anne, LLC under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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