The Dannon Company, Inc. Recall: The label incorrectly states "WALNUT" in the ingredient list and the allergen statement, while the product actually contains PECAN as an ingredient.

🇺🇸 United States

1. January 6, 2017 - Recall initiated
2. February 15, 2017 - Reported by source
3. June 21, 2018 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1440-2017

Event ID

76195

Status

Terminated

Classification

Class II

Company

The Dannon Company, Inc.

Product description

DANONE¿ DAIRY DRINK NUT AND CEREAL 7.7 FL OZ (229mL) bottles, UPC 36632 01421

Quantity

49,360 cases/ 8 HDPE bottles

Reason

The label incorrectly states "WALNUT" in the ingredient list and the allergen statement, while the product actually contains PECAN as an ingredient.

Recall initiation date

January 6, 2017

Report date

February 15, 2017

Classification date

Not published in this source record

Termination date

June 21, 2018

Distribution pattern

Arizona, California, Colorado, Connecticut, Florida, Georgia, Illinois, Indiana, Kansas, Massachusetts, Michigan, North Carolina, New Jersey, New Mexico, New York, Pennsylvania, Texas, Utah

UPC, lot, and code information

Expiration dates: OCT 28 2016 NOV 02 2016 NOV 30 2016 DEC 14 2016 DEC 25 2016 JAN 04 2017 JAN 11 2017 JAN 21 2017 FEB 06 2017 FEB 11 2017 FEB 16 2017 MAR 1 2017

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

Responsible company: The Dannon Company, Inc.

Other recalls from The Dannon Company, 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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