Class ITerminatedVoluntary: Firm initiated

Distribuidora de Alimentos Sendero LLC: food recall H-0648-2026

Distribuidora de Alimentos Sendero LLC of Mission, TX recalled Gorditas de Azucar UPC 860010238134. Reason: Gorditas and Doraditas are missing the following allergens in product label: Wheat and Soy. The FDA listed it as Class I in its Enforcement Report dated Apr 1, 2026; distribution: Texas.

Record status as published: Terminated (terminated Sep 18, 2026). openFDA data last updated Oct 21, 2026.

Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.

Recall details

Product
Gorditas de Azucar UPC 860010238134
Product quantity
2500 units
Reason for recall
Gorditas and Doraditas are missing the following allergens in product label: Wheat and Soy
Codes, lots and dates on the package
All expiration dates
Distribution pattern
Texas
Recalling firm
Distribuidora de Alimentos Sendero LLC, Mission, TX
Classification
Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Voluntary or mandated
Voluntary: Firm initiated
How the firm first notified customers
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Dates

EventDate
Recall initiated by the firmMar 6, 2026
Classified by the FDAApr 3, 2026
Published in the Enforcement ReportApr 1, 2026
TerminatedSep 18, 2026

Other products in the same recall event

The FDA groups related products under one recall event (event 98580).

All food recall records

OpenPlate shows FDA records as published and does not add new findings. Product names and company names belong to their owners.

Sources

  • U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0648-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
  • Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.