So Delicious Dairy Free Salted Caramel Cluster Cashewmilk

WhiteWave - Louisville Pilot Plant has recalled So Delicious Dairy Free Salted Caramel Cluster Cashewmilk, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on January 21, 2026 and was initiated on December 15, 2025. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers So Delicious Dairy Free Salted Caramel Cluster Cashewmilk, with approximately 4,665,608 units distributed in the US; 665,128 units distributed in Canada affected. The company behind the recall is WhiteWave - Louisville Pilot Plant, based in Louisville, CO. The FDA describes the product as: “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…”

Why was So Delicious Dairy Free Salted Caramel Cluster Cashewmilk recalled?

According to the FDA, the stated reason for the recall is: “Foreign material.” In plain terms, this recall relates to foreign material.

A foreign material recall means that pieces of something which should not be in food — such as metal, plastic, or glass — may be present. These can pose a choking hazard or cause injury. Recalls like these are issued to remove the affected product before anyone is hurt.

What should you do?

If you think you may have bought So Delicious Dairy Free Salted Caramel Cluster Cashewmilk, compare it against the product description and identifying codes (***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, 2…) before using it.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact WhiteWave - Louisville Pilot Plant or your local health authority.

About this recall

This recall was distributed in CO. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.