Distribuidora de Alimentos Sendero LLC food recall: Gorditas de Azucar
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Terminated
- Event ID
- 98580
- Recall initiated
- Mar 6, 2026
- Classified by FDA
- Apr 3, 2026
- Posted in Enforcement Report
- Apr 1, 2026
- Terminated
- Sep 18, 2026
- Recalling firm
- Distribuidora de Alimentos Sendero LLC
- Firm location
- Mission, TX, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Products in this event
- 2
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
Gorditas and Doraditas are missing the following allergens in product label: Wheat and Soy
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on Mar 6, 2026. FDA classified it 28 days later, on Apr 3, 2026. This recall event covers 2 separate products, each with its own FDA recall number. Distribution reported by FDA: Texas
Recalled products (2)
H-0648-2026 Class I Terminated
Gorditas de Azucar UPC 860010238134
Codes / lots: All expiration dates
Quantity: 2500 units
H-0649-2026 Class I Terminated
Doraditas de Azucar UPC 5901234123457
Codes / lots: All expiration dates
Quantity: 500 units
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 98580
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.