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CriticalFDAfda-H-0649-2026UNDECLARED ALLERGEN

Doraditas de Azucar UPC 5901234123457

⚠ 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
500
Recall Date
March 6, 2026
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-H-0649-2026.

Gorditas and Doraditas are missing the following allergens in product label: Wheat and Soy

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-H-0649-2026.

Recall ongoing. Follow firm instructions.

✅ 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 Distribuidora De Alimentos Sendero Llc 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-H-0649-2026.

Distribuidora de Alimentos Sendero LLC

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.

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📣 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.

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Distribuidora De Alimentos Sendero Llc Recall FAQ

Distribuidora De Alimentos Sendero Llc is the subject of a food safety report: Doraditas de Azucar UPC 5901234123457. The notice was published on March 6, 2026 by the U.S. Food and Drug Administration (FDA). Approximately 500 units are potentially affected.