Hazelnuts in Shell; packed in a clear plastic bag. 1lb, 5lb, 50lb unit size. No UPC
Summary
The FDA issued a Class III for Hazelnuts in Shell; packed in a clear plastic bag. 1lb, 5lb, 50lb unit size. No by El Ruisenor De Mexico, Inc.. Reason: undeclared allergen ingredient (Hazelnut).
Details
Source
Food Recall
External ID
H-0110-2027
Action Date
2026-10-28
Status
Ongoing
Category
food
Product Description
Hazelnuts in Shell; packed in a clear plastic bag. 1lb, 5lb, 50lb unit size. No UPC
Lot/Code Info: no lot code
Quantity Affected: 20 pounds
Reason for Recall
undeclared allergen ingredient (Hazelnut)
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 III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
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 III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
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-0110-2027" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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