WhiteWave - Louisville Pilot Plant Recall: Foreign material

🇺🇸 United States

1. December 15, 2025 - Recall initiated
2. January 21, 2026 - Reported by source
3. January 29, 2026 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

H-0398-2026

Event ID

98162

Status

Terminated

Classification

Class II

Company

WhiteWave - Louisville Pilot Plant

Product description

So Delicious Dairy Free Salted Caramel Cluster Cashewmilk, Non-Dairy Frozen Dessert, One Pint (473 mL). UPC 744473 476138. Manufactured By/For So Delicious Dairy Free Eugene, OR 97402 So Delicious Dairy Free Salted Caramel Cluster Cashewmilk, Non-Dairy Frozen Dessert. Net wt. 500mL. UPC 744473 276134. Product of the U.S.A. Distributed by Danone Inc., Boucherville, Quebec J4B 1E6

Quantity

4,665,608 units distributed in the US; 665,128 units distributed in Canada

Reason

Foreign material

Recall initiation date

December 15, 2025

Report date

January 21, 2026

Classification date

Not published in this source record

Termination date

January 29, 2026

Distribution pattern

Distributed in the U.S. nationwide and in Canada.

UPC, lot, and code information

UPC 744473; ***In the US*** All Best By dates from 11 DEC 2025 and before 8 AUG 2027 S05-33 25218 20:05 S05-33 is the Plant Code, 25 is the Year, 218 is the Julian Date, 20:05 is the Time of fill. ***In Canada*** BB: 14 Feb 2026 BB: 13 Apr 2026 BB: 14 May 2026 BB: 4 Jun 2026 BB: 31 Jul 2026 BB: 13 Aug 2026 BB: 2 Jan 2027 BB: 3 Jan 2027 BB: 4 Jan 202, BB: 19 Jun 2027 BB: 20 Jun 2027 BB: 21 Jun 2027 BB: 9 Jul 2027 BB: 10 Jul 2027

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: WhiteWave - Louisville Pilot Plant

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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