SunRidge Farms Organic CHILI BEAN BLEND CERTIFIED ORGANIC BY QAI NET WT. 15 LBS Item: 003056 UPC: 086700030561
Summary
The FDA issued a Class III for SunRidge Farms Organic CHILI BEAN BLEND CERTIFIED ORGANIC BY QAI NET WT. 15 LBS by Falcon Trading Co., Inc.. Reason: Potential contamination with pesticides, haloxyfop and thiamethoxam.
Details
Source
Food Recall
External ID
H-0696-2026
Action Date
2026-05-13
Status
Ongoing
Category
food
Product Description
SunRidge Farms Organic CHILI BEAN BLEND CERTIFIED ORGANIC BY QAI NET WT. 15 LBS Item: 003056 UPC: 086700030561
Lot/Code Info: Lots: 3132585, 2652535, 0282570, 2302416.
Quantity Affected: 276 cases (4,140 lbs.)
Reason for Recall
Potential contamination with pesticides, haloxyfop and thiamethoxam
Distribution
U.S. Distribution: CA, CO, HI, MO, TX, VT, WA. Foreign Distribution: None.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-03-24
Company
Royal Oaks, 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 93 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Falcon Trading Co., Inc. has 3 FDA actions in our database, including 3 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 (Falcon Trading Co., Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Falcon Trading Co., Inc. have FDA actions?
Falcon Trading Co., Inc. has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0696-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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