Lower riskFood recall · FDA · Published February 10, 2020
Garza Siete Grain Free Burrito Tortillas Recall: High Sodium Content
Garza Food Ventures recalls Siete Grain Free Burrito Size Tortillas due to high sodium content (340mg/serving vs 15mg declared). Consumers should check UPC 865336000083 for affected products.
“Garza Siete Grain Free Burrito Tortillas Recall: High Sodium Content.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/15951-garza-siete-grain-free-burrito-tortillas-recall-high-sodium-content. Based on FDA recall #F-0826-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0826-2020%22&limit=1).
The Food and Drug Administration announced on Feb. 10, 2020, that Garza Food Ventures voluntarily recalled Siete Grain Free Burrito Size Tortillas due to undeclared sodium levels, according to FDA records.
How to tell if you have it
Brand: Siete
Product: Grain Free Burrito Size Tortillas Net Wt 15 oz (423g) 6 count
The sodium level in the product is 340 mg per serving, instead of the 15 mg declared on the label, according to the FDA.
Context
GovInfoNow's records show Garza Food Ventures has one other recall on record since May 15, 2020. On May 15, 2020, the company issued a recall for Garza Siete Grain Free Cashew Flour Tortillas due to potential foreign material risk. Other recent recalls of similar products include Spicy Breakfast Burrito Recall (Dec. 5, 2025), MG Foods Spicy Breakfast Burrito Recall (Jan. 13, 2026) and Spicy Breakfast Burrito Recall (July 18, 2026).
How to tell if you have this one
Check for the UPC 865336000083 on the flexible plastic packaging. The product is sold in 6-count packages labeled as 'Siete Grain Free Burrito Size Tortillas' with specific lot codes like L0219CB through A2420CB.
Brand
Garza Food Ventures
Product
Siete Grain Free Burrito Size Tortillas Net Wt 15 oz (423g) 6 count UPC 865336000083 packaged in flexible plastic
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the UPC 865336000083 on the flexible plastic packaging to confirm if the product is affected.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “Available Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 57 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-0826-2020 (February 10, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0826-2020 to see it in context.
Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.