Class IITerminatedVoluntary: Firm initiated
WhiteWave - Louisville Pilot Plant: food recall H-0398-2026
WhiteWave - Louisville Pilot Plant of Louisville, CO recalled So Delicious Dairy Free Salted Caramel Cluster Cashewmilk, Non-Dairy Frozen Dessert, One Pint (473 mL). UPC 744473… Reason: Foreign material. The FDA listed it as Class II in its Enforcement Report dated Jan 21, 2026; distribution: nationwide.
Record status as published: Terminated (terminated Jan 29, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 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
- Product quantity
- 4,665,608 units distributed in the US; 665,128 units distributed in Canada
- Reason for recall
- Foreign material
- Codes, lots and dates on the package
- ***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
- Distribution pattern
- Distributed in the U.S. nationwide and in Canada.
- Recalling firm
- WhiteWave - Louisville Pilot Plant, Louisville, CO
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Dec 15, 2025 |
| Classified by the FDA | Jan 14, 2026 |
| Published in the Enforcement Report | Jan 21, 2026 |
| Terminated | Jan 29, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0398-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.