So Delicious Dairy Free Salted Caramel Cluster Cashewmilk, Non-Dairy Frozen Dessert, One Pint (473 mL). UPC 744473 47613
Summary
The FDA issued a Class II for So Delicious Dairy Free Salted Caramel Cluster Cashewmilk, Non-Dairy Frozen Dess by WhiteWave - Louisville Pilot Plant. Reason: Foreign material.
Details
Source
Food Recall
External ID
H-0398-2026
Action Date
2026-01-21
Status
Terminated
Category
food
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
Lot/Code Info: ***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
Quantity Affected: 4,665,608 units distributed in the US; 665,128 units distributed in Canada
Reason for Recall
Foreign material
Distribution
Distributed in the U.S. nationwide and in Canada.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-12-15
Company
Louisville, CO
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 54 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (WhiteWave - Louisville Pilot Plant) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does WhiteWave - Louisville Pilot Plant have FDA actions?
This is the only FDA action we have on record for WhiteWave - Louisville Pilot Plant in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0398-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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