Trail Toddy & Company LLC Recall: Cream is declared in the Ingredients statement and Dairy is declared in the Contains statement. Milk is not declared.

🇺🇸 United States

1. November 9, 2021 - Recall initiated
2. December 8, 2021 - Reported by source
3. May 6, 2022 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0222-2022

Event ID

89022

Status

Terminated

Classification

Class II

Company

Trail Toddy & Company LLC

Product description

Classic Irish Coffee Hint of Cocoa, each packet weighs 1.09 oz (31g), 30 packets per case. UPC 8 60003 91545 5. This product is a blend of shelf-stable ingredients and contains no alcohol. The label is read in parts: "***Ingredients: CANE SUGAR, *CREAM POWDER, *COFFEE, COCOA POWDER, MOLASSES, HONEY, VANILLA, SEA SALT, LOCUST BEAN GUM, *SILICON DIOXIDE. *ORGANIC INGREDIENT.***CONTAINS DAIRY***".

Quantity

20 packets

Reason

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

Recall initiation date

November 9, 2021

Report date

December 8, 2021

Classification date

Not published in this source record

Termination date

May 6, 2022

Distribution pattern

distributed in Illinois and Montana, and Massachusetts

UPC, lot, and code information

Best by all of September 2022.

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 89022 with 2 other product entries in Public Health Trace.

Responsible company: Trail Toddy & Company LLC

Other recalls from Trail Toddy & Company LLC

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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