Fresh Recalls

FDAClass III · Food · Recall H-1236-2026 · Recalled August 12, 2026

Kanni Delight 31/40 Fresh Frozen Vannamei White Shrimp IQF recall — CAMPO RICO FOODS LLC

Agency report date: August 12, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Kanni Delight 31/40 Fresh Frozen Vannamei White Shrimp IQF
Company / brand
CAMPO RICO FOODS
Lot / serial / date codes
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
LA
Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Nitrofurans detected in product

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class III: not likely to cause adverse health consequences.

Affected product: Kanni Delight 31/40 Fresh Frozen Vannamei White Shrimp IQF

3. Open the official notice or contact

Official recall ID
H-1236-2026
Brand
CAMPO RICO FOODS
Classification
Class III
Units affected
11 cases
Recall status
Completed
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Metairie, LA, United States
Firm address
2309 L And A Rd, 70001-5955

Identifying details (verbatim from the notice)

Product codes / lots
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
LA
Firm notified the public via
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
FDA event ID
99451
Recall initiated
June 18, 2026
FDA classified
August 17, 2026
FDA report date
August 12, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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