Kanni Delight 31/40 Fresh Frozen Vannamei White Shrimp IQF
Recalled by CAMPO RICO FOODS LLC
Food recall
CAMPO RICO FOODS LLC
Class III — least serious
Using this product is not likely to cause health problems, but it breaks an FDA rule (for example, a labeling or packaging issue).
CAMPO RICO FOODS LLC has recalled Kanni Delight 31/40 Fresh Frozen Vannamei White Shrimp IQF, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on August 12, 2026 and was initiated on June 18, 2026. It is classified as a Class III recall, which means using this product is not likely to cause health problems, but it breaks an FDA rule (for example, a labeling or packaging issue).
Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.
What was recalled?
This recall covers Kanni Delight 31/40 Fresh Frozen Vannamei White Shrimp IQF, with approximately 11 cases affected. The company behind the recall is CAMPO RICO FOODS LLC, based in Metairie, LA. The FDA describes the product as: “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”
Why was Kanni Delight 31/40 Fresh Frozen Vannamei White Shrimp IQF recalled?
According to the FDA, the stated reason for the recall is: “Nitrofurans detected in product.”
What should you do?
If you think you may have bought Kanni Delight 31/40 Fresh Frozen Vannamei White Shrimp IQF, compare it against the product description and identifying 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 Regi…) before using it.
The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact CAMPO RICO FOODS LLC or your local health authority.
About this recall
This recall was distributed in LA. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.
Who this recall affects
This recall matters to anyone who bought Kanni Delight 31/40 Fresh Frozen Vannamei White Shrimp IQF. Even if you feel fine, it's worth checking what you have on hand rather than assuming you were missed.
Distribution listed in the notice: LA.
How to check whether you have it
On packaged food, lot codes and best-by dates are usually printed in small date-coding ink on the side seam, the bottom of the package, or near the top seal — not on the front label. The UPC barcode is on the back or bottom.
Compare what you find against the identifying details in this recall: 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
What to do if you already bought it
Do not eat the product, even if it looks and smells normal — contamination is usually invisible.
Return it to the store for a refund, or throw it away in a sealed bag so pets and wildlife can't reach it.
If it touched other food or surfaces, wash those surfaces and your hands with hot soapy water. When in doubt, contact CAMPO RICO FOODS LLC or your local health department.
Full recall details
- Status
- Completed
- Date reported
- August 12, 2026
- Recall started
- June 18, 2026
- Distributed in
- LA
What you can do
Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.
Quick answers
Why was Kanni Delight 31/40 Fresh Frozen Vannamei White Shrimp IQF recalled?+
According to the FDA: Nitrofurans detected in product
How serious is this recall?+
Class III — least serious. Using this product is not likely to cause health problems, but it breaks an FDA rule (for example, a labeling or packaging issue).
What should I do if I have Kanni Delight 31/40 Fresh Frozen Vannamei White Shrimp IQF?+
Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: H-1236-2026. Information last synced from the FDA on August 25, 2026.