Cafe' Intermezzo Cookie Dough Cheesecake Recalled for Incomplete Sub-Ingredient Labeling
Epic Baking recalls 102 units of Cafe' Intermezzo Cookie Dough Cheesecake distributed to Georgia and Tennessee due to incomplete sub-ingredient labeling. All major allergens are properly disclosed.
What this means for you
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: FDA Class III recall with no reported illnesses or injuries. The issue is incomplete sub-ingredient disclosure on labeling, though all major allergens are properly listed in the ingredient statement.
Plain-English summary
Epic Baking is recalling 102 units of Cafe' Intermezzo Cookie Dough Cheesecake (7.5 lbs each) with product codes CKD110822 to CKD122822. The product contains cream cheese, eggs, sugar, whipped cream, chocolate ganache, cocoa crust, chocolate-dipped cookies, cookie dough filling, vanilla extract, and corn starch. The product contains milk, eggs, wheat, and soy, and may contain tree nuts and peanuts.
The recall was initiated because the manufacturer did not separately list sub-ingredients on the product label. However, all major allergens are properly disclosed in both the ingredient statement and the "Contains" statement.
The affected product was distributed to Georgia and Tennessee. No illnesses or injuries have been reported.
The recalled product
- Product
- Cafe' Intermezzo Cookie Dough Cheesecake 7.5 lbs Ingredients: Cream Cheese, Eggs, Sugar, Whipped Cream, Chocolate Ganache (Chocolate Chips, Heavy Cream), Cocoa Crust (Graham Crackers, Butter, Sugar, Cocoa Powder, Vanilla Extract), Chocolate-Dipped Cookies (Chocolate Chips, Butter
- Manufacturer
- Epic Baking
- Hazard
- Affected units
- 102
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 (1)
- CKD110822 to CKD122822
Distribution
Part of a larger recall action
This product is one of 23 recalled by Epic Baking 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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