Tres Latin Foods Pupusas, Stuffed Corn Tortillas with Black Bean & Sweet Corn, Net Wt. 10oz (283g), UPC 85443000237. Keep Frozen [4] 2.5...
⚠ 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-0116-2018.
Tres Latin Foods is recalling specific code dates of Kale & Pinto Bean 10 oz. Pupusas and Black Bean and Sweet Corn 10 oz. Pupusas due to undeclared milk allergen.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0116-2018.
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 Tres Latin Foods 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-0116-2018.
Tres Latin Foods
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.
Tres Latin Foods Recall FAQ
Tres Latin Foods is the subject of a frozen food safety report: Tres Latin Foods Pupusas, Stuffed Corn Tortillas with Black Bean & Sweet Corn, Net Wt. 10oz (283g), UPC 85443000237. Keep Frozen [4] 2.5.... The notice was published on October 21, 2017 by the U.S. Food and Drug Administration (FDA). Approximately 533 units are potentially affected.