Fritura mixed dry fruit; packed in a clear plastic 1lb, 5lb, 25lb unit sizes. no UPC
Summary
The FDA issued a Class II for Fritura mixed dry fruit; packed in a clear plastic 1lb, 5lb, 25lb unit sizes. no by El Ruisenor De Mexico, Inc.. Reason: undeclared allergen ingredient (Wheat, Yellow #5, Yellow #6).
Details
Source
Food Recall
External ID
H-0120-2027
Action Date
2026-10-28
Status
Ongoing
Category
food
Product Description
Fritura mixed dry fruit; packed in a clear plastic 1lb, 5lb, 25lb unit sizes. no UPC
Lot/Code Info: no lot code
Quantity Affected: 134.59 pounds
Reason for Recall
undeclared allergen ingredient (Wheat, Yellow #5, Yellow #6)
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
Company
Vernon, CA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
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 II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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-0120-2027" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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