RecallHawk
Class I Recall

Fritura Rueda Papa / Potato Wheel Snack; packed in a clear plastic 1lb, 5lb, 33lb unit sizes. No UPC

El Ruisenor De Mexico, Inc.

Summary

The FDA issued a Class I for Fritura Rueda Papa / Potato Wheel Snack; packed in a clear plastic 1lb, 5lb, 33l by El Ruisenor De Mexico, Inc.. Reason: undeclared allergen ingredient (Wheat).

Details

Source

Food Recall

External ID

H-0123-2027

Action Date

2026-10-28

Status

Ongoing

Category

food

Product Description

Fritura Rueda Papa / Potato Wheel Snack; packed in a clear plastic 1lb, 5lb, 33lb unit sizes. No UPC

Lot/Code Info: lot code: 069 2 26 1 020

Quantity Affected: 260.16 pounds

Reason for Recall

undeclared allergen ingredient (Wheat)

Distribution

Recalling firm distributes primarily to California customers both retail and wholesale. Additional distribution to limited customers in Hawaii, Illinois, Kansas, Nevada, Oregon, and Washington.

Type: Voluntary: Firm initiated

Recall Initiated: 2026-08-24

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 82 food recalls issued in the same week, part of 117 food-related FDA actions this month.

El Ruisenor De Mexico, Inc. has 61 FDA actions in our database, including 61 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 (El Ruisenor De Mexico, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does El Ruisenor De Mexico, Inc. have FDA actions?

El Ruisenor De Mexico, Inc. has 61 FDA actions in our database, including 61 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0123-2027" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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