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Class IITerminated in FDA datasetRecall initiated Nov 9, 2021

Mocha Irish Coffee 66% Cocao, each packet weighs 1.41 oz (40g), 30 packets per case.

Recalling firm: Trail Toddy & Company LLC

Why it was recalled

Cream is declared in the Ingredients statement and Dairy is declared in the Contains statement. Milk is not declared.

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: May 6, 2022.

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

ProductMocha Irish Coffee 66% Cocao, each packet weighs 1.41 oz (40g), 30 packets per case. UPC 8 60003 91547 9. The label is read in parts: "***Ingredients: CANE SUGAR, *CREAM POWDER, COCOA BEANS, COCOA BUTTER, *COFFEE, COCOA POWDER, MOLASSES, HONEY, VANILLA, SEA SALT, LOCUST BEAN GUM, SILICON DIOXIDE, SOY LECITHIN.***CONTAINS DAIRY***".
Package size1.41 oz
UPC860003915479

FDA code information

Best by all of September 2022.

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

Full FDA record and distribution details

Original product description

Mocha Irish Coffee 66% Cocao, each packet weighs 1.41 oz (40g), 30 packets per case. UPC 8 60003 91547 9. The label is read in parts: "***Ingredients: CANE SUGAR, *CREAM POWDER, COCOA BEANS, COCOA BUTTER, *COFFEE, COCOA POWDER, MOLASSES, HONEY, VANILLA, SEA SALT, LOCUST BEAN GUM, SILICON DIOXIDE, SOY LECITHIN.***CONTAINS DAIRY***".

Extracted codes and context

TypeCode / valueContext
UPC860003915479sh Coffee 66% Cocao, each packet weighs 1.41 oz (40g), 30 packets per case. UPC 8 60003 91547 9. The label is read in parts: "***Ingredients: CANE SUGAR, *CREAM POWDER, COCOA BEANS, COCOA BUTTER, *COFFEE, COCOA POW

Original FDA recall reason

Cream is declared in the Ingredients statement and Dairy is declared in the Contains statement. Milk is not declared.

Recall details

Recall number
F-0223-2022
Event ID
89022
FDA status
Terminated
Initiated
Nov 9, 2021
Reported
Dec 8, 2021
Classified
Nov 30, 2021
Terminated
May 6, 2022
Quantity
50 packets
Location
Tillamook, OR, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

distributed in Illinois and Montana, and Massachusetts

FDA source record · F-0223-2022

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

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