Class ITerminated in FDA datasetRecall initiated Nov 9, 2017

Dilettante Chocolates Espresso Blend, Espresso Beans in Semisweet, Milk and White Chocolate.,…

Recalling firm: Seattle Gourmet Foods Inc.

Why it was recalled

Costco item # 2335, Dilettante Chocolates Espresso Blend, Espresso Beans in Semisweet, Milk and White Chocolate is recalled because it may contain undeclared almonds.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jan 8, 2018.

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Compare the exact product and package details with the label you have.

ProductDilettante Chocolates Espresso Blend, Espresso Beans in Semisweet, Milk and White Chocolate., Costco item # 2335. The product is packaged in a clear plastic bag, net weight 5-pounds and has the UPC 37041 05211. The product label is read in parts: "***Dilettante Chocolates, Kent WA 98032, Dilettante Chocolates 19016 72nd Ave South Kent, WA 98144***".

FDA code information

Lot Code 12287 and BEST BY 021619. The word lot code is not listed on the label.

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Dilettante Chocolates Espresso Blend, Espresso Beans in Semisweet, Milk and White Chocolate., Costco item # 2335. The product is packaged in a clear plastic bag, net weight 5-pounds and has the UPC 37041 05211. The product label is read in parts: "***Dilettante Chocolates, Kent WA 98032, Dilettante Chocolates 19016 72nd Ave South Kent, WA 98144***".

Original FDA recall reason

Costco item # 2335, Dilettante Chocolates Espresso Blend, Espresso Beans in Semisweet, Milk and White Chocolate is recalled because it may contain undeclared almonds.

Recall details

Recall number
F-0393-2018
Event ID
78547
FDA status
Terminated
Initiated
Nov 9, 2017
Reported
Nov 29, 2017
Classified
Nov 28, 2017
Terminated
Jan 8, 2018
Quantity
127 cases (6/5 lbs. bags per case)
Location
Tukwila, WA, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

distributed in Utah and Washington

FDA source record · F-0393-2018

Data updated September 16, 2026. View official FDA data ↗

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