Blue Bell Creameries, L.P. Recall: All ice cream products, Chocolate Chip Cookie Dough, Cookie Two Step ice Cream, Krazy Kookie Dough, and Blue Monster, containing cookie dough supplied by Aspen Hills, Inc., due to the potential for them to contain Listeria monocytogenes.

🇺🇸 United States

1. September 20, 2016 - Recall initiated
2. January 18, 2017 - Reported by source
3. July 18, 2017 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0876-2017

Event ID

75254

Status

Terminated

Classification

Class I

Company

Blue Bell Creameries, L.P.

Product description

BLUE BELL(R) ICE CREAM Krazy Kookie Dough, 3 Gallons

Quantity

3699 units

Reason

All ice cream products, Chocolate Chip Cookie Dough, Cookie Two Step ice Cream, Krazy Kookie Dough, and Blue Monster, containing cookie dough supplied by Aspen Hills, Inc., due to the potential for them to contain Listeria monocytogenes.

Recall initiation date

September 20, 2016

Report date

January 18, 2017

Classification date

Not published in this source record

Termination date

July 18, 2017

Distribution pattern

Alabama, Florida, Georgia, Kentucky, Louisiana, Mississippi, North Carolina, South Carolina, Tennessee, and Virginia

UPC, lot, and code information

all codes

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

Other products recalled under this same event

This recall shares FDA event ID 75254 with 3 other product entries in Public Health Trace.

Responsible company: Blue Bell Creameries, L.P.

Other recalls from Blue Bell Creameries, L.P.

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 I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

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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