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FDA source record Class II Terminated

Cafe' Intermezzo White Chocolate Amaretto Cheesecake 7 lbs Ingredients: Eggs, Cream Cheese, Sugar, Amaretto Syrup, Whipped Cream, Almond Crust (Graham Crackers, Butter, Sugar, A...

Recall Date: 2023-01-30 Recalling Firm: Epic Baking Record Ref: F-0605-2023

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns Cafe' Intermezzo White Chocolate Amaretto Cheesecake 7 lbs Ingredients: Eggs, Cream Cheese, Sugar, Amaretto Syrup, Whipped Cream, Almond Crust (Graham Crackers, Butter, Sugar, A... and names Epic Baking as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: Epic Baking
  • Classification: Class II
  • Status: Terminated
  • Recall date: 2023-01-30
Best identifiers to check for a FDA record

Compare UPC/GTIN, lot or batch code, package size, flavor or variety, and any best-by/use-by date listed in the notice.

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Product Description & Identification

Cafe' Intermezzo White Chocolate Amaretto Cheesecake 7 lbs Ingredients: Eggs, Cream Cheese, Sugar, Amaretto Syrup, Whipped Cream, Almond Crust (Graham Crackers, Butter, Sugar, Almonds, Vanilla Extract), Vanilla Extract, White Chocolate, Almond Extract, Corn Starch. Contains: Milk, eggs, wheat, and soy. May contain tree nuts and peanuts.

Reason for Recall / Hazard Identified

Label does not list sub ingredients that include allergens. Label states, "May contain tree nuts" when the product actually contains almonds.

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.

Consumer Action Recorded in the Source

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Distribution & Affected States

Product was shipped to the following states GA & TN

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
F-0605-2023
Indexed update
2026-08-09 21:59:13 UTC
Official source
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