Fiesta Mix 25 pound bags, with UPC 032491208597. The product is labeled in part: "***Fiesta Mix A Blend of the Sweet Crunchy and Salt...
⚠ 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.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0634-2013.
Fiesta Mix product is recalled due to undeclared soy, milk, wheat, and FD& C Yellow #6 on finished product label.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0634-2013.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact The Nut Factory Inc. or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- 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-0634-2013.
The Nut Factory Inc.
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.
The Nut Factory Inc. Recall FAQ
The Nut Factory Inc. is the subject of a seafood safety report: Fiesta Mix 25 pound bags, with UPC 032491208597. The product is labeled in part: "***Fiesta Mix A Blend of the Sweet Crunchy and Salt.... The notice was published on October 17, 2012 by the U.S. Food and Drug Administration (FDA). Approximately 13 units are potentially affected.