Casper's Ice Cream, Inc Recall: Burnt Almond Fudge ice cream was packaged into Canadian Vanilla tubs during the run of the Burnt Almond Fudge. The Canadian Vanilla tubs do not list tree nut (almond) allergen in the ingredients list or contains statement leading to undeclared allergens.

🇺🇸 United States

1. May 24, 2022 - Recall initiated
2. June 29, 2022 - Reported by source
3. August 31, 2022 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1345-2022

Event ID

90294

Status

Terminated

Classification

Class II

Company

Casper's Ice Cream, Inc

Product description

Red Button Vintage Creamery Canadian Vanilla Ice Cream, 56 ounce tub, UPC 0 77865 01001 7, Distributed by Associated Foods Stores, Salt Lake City, UT, 84119. Store Frozen.

Quantity

1680 cases of 6 tubs each

Reason

Burnt Almond Fudge ice cream was packaged into Canadian Vanilla tubs during the run of the Burnt Almond Fudge. The Canadian Vanilla tubs do not list tree nut (almond) allergen in the ingredients list or contains statement leading to undeclared allergens.

Recall initiation date

May 24, 2022

Report date

June 29, 2022

Classification date

Not published in this source record

Termination date

August 31, 2022

Distribution pattern

Nationwide.

UPC, lot, and code information

Lot # 344-21-946 Best by date: 12/10/2024

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: Casper's Ice Cream, Inc

Other recalls from Casper's Ice Cream, Inc

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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