Class IIICompletedVoluntary: Firm initiated

CAMPO RICO FOODS LLC: food recall H-1236-2026

CAMPO RICO FOODS LLC of Metairie, LA recalled Kanni Delight 31/40 Fresh Frozen Vannamei White Shrimp IQF, Raw Peeled & Deveined Tail Off, Gross Weight: 5 lb.,… Reason: Nitrofurans detected in product. The FDA listed it as Class III in its Enforcement Report dated Aug 12, 2026; distribution: Louisiana.

Record status as published: Completed. openFDA data last updated Oct 21, 2026.

Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.

Recall details

Product
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
Product quantity
11 cases
Reason for recall
Nitrofurans detected in product
Codes, lots and dates on the package
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
Distribution pattern
LA
Recalling firm
CAMPO RICO FOODS LLC, Metairie, LA
Classification
Class III — the FDA uses this class for a situation in which using or being exposed to the product is not likely to cause adverse health consequences.
Voluntary or mandated
Voluntary: Firm initiated
How the firm first notified customers
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Dates

EventDate
Recall initiated by the firmJun 18, 2026
Classified by the FDAAug 17, 2026
Published in the Enforcement ReportAug 12, 2026

All food recall records

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Sources

  • U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-1236-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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