Skip to main content
CriticalFDAfda-F-1162-2020UNDECLARED ALLERGEN

Earth Grown brand Vanilla Non-Dairy Frozen Dessert in pint sized paperboard carton with a paperboard lid.

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (undeclared allergen). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Category
Units Affected
72,288
Recall Date
July 29, 2020
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1162-2020.

Undeclared cashews in the product.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1162-2020.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Smith Foods Inc. or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1162-2020.

Smith Foods Inc.

FDA

About the U.S. Food and Drug Administration

The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

Visit FDA.gov →

📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

How to report to FDAFile a report at FDA

Smith Foods Inc. Recall FAQ

Smith Foods Inc. is the subject of a dairy safety report: Earth Grown brand Vanilla Non-Dairy Frozen Dessert in pint sized paperboard carton with a paperboard lid.. The notice was published on July 29, 2020 by the U.S. Food and Drug Administration (FDA). Approximately 72,288 units are potentially affected.