RecallRadar
High RiskReported April 1, 2026

Doraditas de Azucar UPC 5901234123457

Recalled by Distribuidora de Alimentos Sendero LLC

Product image for Doraditas de Azucar UPC 5901234123457
Product image via Open Food Facts. It may show general packaging and not the exact recalled lot — always confirm using the codes below.

Class I — most serious

There is a reasonable chance that using this product could cause serious health problems or death.

See all recalls involving an undeclared allergen

Distribuidora de Alimentos Sendero LLC has recalled Doraditas de Azucar UPC 5901234123457, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on April 1, 2026 and was initiated on March 6, 2026. It is classified as a Class I recall, which means there is a reasonable chance that using this product could cause serious health problems or death.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers Doraditas de Azucar UPC 5901234123457, with approximately 500 units affected. The company behind the recall is Distribuidora de Alimentos Sendero LLC, based in Mission, TX. The FDA describes the product as: “Doraditas de Azucar UPC 5901234123457”

Why was Doraditas de Azucar UPC 5901234123457 recalled?

According to the FDA, the stated reason for the recall is: “Gorditas and Doraditas are missing the following allergens in product label: Wheat and Soy.” In plain terms, this recall relates to an undeclared ingredient or allergen.

An undeclared ingredient means a food contains something — often a major allergen such as milk, eggs, soy, wheat, peanuts, or tree nuts — that is not listed on the label. For most people this is not dangerous, but for someone with a food allergy or sensitivity it can trigger a serious reaction. Accurate labeling is required so that people can avoid ingredients they need to stay away from.

What should you do?

If you think you may have bought Doraditas de Azucar UPC 5901234123457, compare it against the product description and identifying codes (All expiration dates) before using it.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Distribuidora de Alimentos Sendero LLC or your local health authority.

About this recall

This recall was distributed in TX. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.

Full recall details

Status
Completed
Date reported
April 1, 2026
Recall started
March 6, 2026
Distributed in
TX
What was recalled
Doraditas de Azucar UPC 5901234123457
Why it was recalled (as stated by the FDA)
Gorditas and Doraditas are missing the following allergens in product label: Wheat and Soy
How to identify the affected product
All expiration dates
Amount recalled
500 units

What you can do

Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.

Quick answers

Why was Doraditas de Azucar UPC 5901234123457 recalled?+

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

How serious is this recall?+

Class I — most serious. There is a reasonable chance that using this product could cause serious health problems or death.

What should I do if I have Doraditas de Azucar UPC 5901234123457?+

Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.

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View the official FDA record

Opens the U.S. Food and Drug Administration (FDA) data for this recall.

Recall number: H-0649-2026. Information last synced from the FDA on July 6, 2026.

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