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Use caution Food recall · FDA · Published February 25, 2020

Les Chateaux De France Recalls Butterfly Shrimp for Undeclared Sulfites

Les Chateaux De France recalls 50 lb. cases of Butterfly Shrimp due to undeclared sodium metabisulfite, which can cause allergic reactions in sensitive individuals.

🇺🇸 FDA recall #F-0841-2020FoodLes Chateaux De France ›
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Recalling firmLes Chateaux De France1 Craft Ave · Inwood, NY 11096-1609
✎ GovInfoNow plain-language explainer

What happened, in plain English

Les Chateaux De France is recalling Butterfly Shrimp 16/20 sold in 50 lb. cases because the product contains undeclared sodium metabisulfite. This ingredient is a sulfite that can trigger severe allergic or anaphylactic reactions in people with sulfite sensitivity. The recall covers specific lots distributed to several states. Read more at govinfonow.com/recall/15836-les-chateaux-de-france-recalls-butterfly-shrimp-for-undeclared-sulfites.

Source Summary by GovInfoNow · govinfonow.com/recall/15836-les-chateaux-de-france-recalls-butterfly-shrimp-for-undeclared-sulfites · Updated October 11, 2026 · FDA enforcement record: FDA #F-0841-2020

Cite this page

“Les Chateaux De France Recalls Butterfly Shrimp for Undeclared Sulfites.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/15836-les-chateaux-de-france-recalls-butterfly-shrimp-for-undeclared-sulfites. Based on FDA recall #F-0841-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0841-2020%22&limit=1).

Why it’s dangerous

Sodium metabisulfite is a preservative that can cause serious allergic-type reactions, including anaphylaxis, in sensitive individuals. Because the ingredient was not declared on the label, consumers with sulfite allergies were unaware of the risk and could have consumed it unknowingly.

Who’s affected

Consumers who purchased the recalled Butterfly Shrimp cases, particularly those with known sulfite allergies or sensitivities. The product was distributed to Nevada, Florida, New York, Pennsylvania, Louisiana, New Jersey, Arizona, and Massachusetts.

How to tell if you have this one

Check for Butterfly Shrimp 16/20 packed in 50 lb. cases. Look for case dates of 2-20-20, 2-13-20, or 1-30-20. The product was distributed to NV, FL, NY, PA, LA, NJ, AZ, and MA.

  • Brand
    Les Chateaux De France
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check your inventory

    Verify if you have Butterfly Shrimp 16/20 in 50 lb. cases with case dates of 2-20-20, 2-13-20, or 1-30-20.

  2. Do not consume

    If you have the recalled product, do not eat it due to the undeclared sulfite risk.

Where it went and when

Where it was distributed

Distributed in 8 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: yesMAOregon: not listedORNevada: yesNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: yesPANew Jersey: yesNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: yesAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: yesLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: yesFL

FDA distribution: “NV, FL, NY, PA, LA, NJ, AZ, MA” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, Florida, Louisiana, Massachusetts, Nevada, New Jersey, New York, Pennsylvania.

Recall timeline

FDA terminated this recall 6 months after the firm started it.

1. Firm started the recall: Feb 25, 202012. FDA classified it Class II: Mar 17, 202023. Published in FDA’s Enforcement Report: Mar 18, 202034. FDA terminated the recall: Sep 1, 202042020
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-0841-2020 (February 25, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0841-2020 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA