Kanni Delight 31/40 Fresh Frozen Vannamei White Shrimp IQF, Raw Peeled & Deveined Tail Off, Gross Weight: 5 lb., package
Summary
The FDA issued a Class III for Kanni Delight 31/40 Fresh Frozen Vannamei White Shrimp IQF, Raw Peeled & Deveine by CAMPO RICO FOODS LLC. Reason: Nitrofurans detected in product.
Details
Source
Food Recall
External ID
H-1236-2026
Action Date
2026-08-12
Status
Completed
Category
food
Product Description
Kanni Delight 31/40 Fresh Frozen Vannamei White Shrimp IQF, Raw Peeled & Deveined Tail Off, Gross Weight: 5 lb., packaged in polyethylene bags, packed 6 bags per case, Product of India, Farm Raised, for food service only
Lot/Code Info: Batch: 6D08 Code: 6A14 and Farm Registration Number: TN000643/006 Code: 6A21 and Farm Registration Numbers: TN000643/006, TN000643/007 Code: 6A25 and Farm Registration Number: TN000603/002 Best-by/Expiration Date: April 7, 2028 Approval No. 941
Quantity Affected: 11 cases
Reason for Recall
Nitrofurans detected in product
Distribution
LA
Type: Voluntary: Firm initiated
Recall Initiated: 2026-06-18
Company
Metairie, LA
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 37 food recalls issued in the same week, part of 54 food-related FDA actions this month.
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 (CAMPO RICO FOODS LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does CAMPO RICO FOODS LLC have FDA actions?
This is the only FDA action we have on record for CAMPO RICO FOODS LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-1236-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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