RecallHawk
Class I Recall

Doraditas de Azucar UPC 5901234123457

Distribuidora de Alimentos Sendero LLC

Summary

The FDA issued a Class I for Doraditas de Azucar UPC 5901234123457 by Distribuidora de Alimentos Sendero LLC. Reason: Gorditas and Doraditas are missing the following allergens in product label: Wheat and Soy.

Details

Source

Food Recall

External ID

H-0649-2026

Action Date

2026-04-01

Status

Completed

Category

food

Product Description

Doraditas de Azucar UPC 5901234123457

Lot/Code Info: All expiration dates

Quantity Affected: 500 units

Reason for Recall

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

Distribution

Texas

Type: Voluntary: Firm initiated

Recall Initiated: 2026-03-06

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 64 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Distribuidora de Alimentos Sendero LLC has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Distribuidora de Alimentos Sendero LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Distribuidora de Alimentos Sendero LLC have FDA actions?

Distribuidora de Alimentos Sendero LLC has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0649-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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