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Lower risk Food recall · FDA · Published November 21, 2019

Endorphin Farms Tobago Keys Dipping Sauce Recall: Undeclared Fish Allergen

Endorphin Farms recalls Tobago Keys Coral Ridge Seafood Dipping Sauce and Peruvian Gold Grilling Sauce due to undeclared fish allergen in labels.

🇺🇸 FDA recall #F-0560-2020FoodEndorphin Farms ›
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Recalling firmEndorphin Farms, Inc.3255 Parker Dr · Saint Augustine, FL 32084-0892
✎ GovInfoNow plain-language explainer

Endorphin Farms is recalling two seafood sauces because their labels were applied to the wrong products, creating an undeclared fish allergen. This poses a risk for people with fish allergies who might consume the sauce without knowing. Read more at govinfonow.com/recall/16248-endorphin-farms-tobago-keys-dipping-sauce-recall-undeclared-fish-allergen.

Source Summary by GovInfoNow · govinfonow.com/recall/16248-endorphin-farms-tobago-keys-dipping-sauce-recall-undeclared-fish-allergen · Updated October 5, 2026 · FDA enforcement record: FDA #F-0560-2020

Cite this page

“Endorphin Farms Tobago Keys Dipping Sauce Recall: Undeclared Fish Allergen.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/16248-endorphin-farms-tobago-keys-dipping-sauce-recall-undeclared-fish-allergen. Based on FDA recall #F-0560-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0560-2020%22&limit=1).

The FDA announced on 2019-11-21 that Endorphin Farms, Inc. voluntarily recalled Tobago Keys brand Coral Ridge Seafood Dipping Sauce and Peruvian Gold Grilling Sauce due to undeclared fish allergens from mislabeled products.

How to tell if you have it

  • Brand: Tobago Keys
  • Products: Coral Ridge Seafood Dipping Sauce 12 FL.OZ. (355 ml), Peruvian Gold Grilling Sauce 12 FL.OZ (355 ml)
  • Lot code: TTPGOCT092021EF

The hazard

Product labels were applied to the wrong product, resulting in an undeclared fish allergen.

Context

GovInfoNow's records show other recent recalls of similar products include Anthony's BBQ Sauce Recall: Undeclared Fish Allergen in 15oz Bottle (2025-11-07), Booey's Dragon's Breath Sauce Recall: Undeclared Fish and Sesame (2026-03-23), and Eunha Fisheries FLOUNDER SASHIMI With Undeclared Allergens - Recall (2026-07-01).

How to tell if you have this one

Check for the product code TTPGOCT092021EF on the label. The sauces are sold in 12 fl.oz. (355 ml) containers under the Tobago Keys brand.

  • Brand
    Endorphin Farms
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Labels

    Look for the product code TTPGOCT092021EF on the label to confirm if the sauce is recalled.

Where it went and when

Where it was distributed

Distributed in Florida and North Carolina.

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: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: yesNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: yesFL

FDA distribution: “Product was distributed to 4 consignees, 3 in Florida and one in North Carolina.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Florida, North Carolina.

Recall timeline

FDA terminated this recall 7 months after the firm started it.

1. Firm started the recall: Nov 21, 201912. Published in FDA’s Enforcement Report: Jan 22, 202023. FDA classified it Class II: Jan 24, 202034. FDA terminated the recall: Jun 8, 2020420192020
  1. Firm started the recall
  2. Published in FDA’s Enforcement Report
  3. FDA classified it Class II
  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-0560-2020 (November 21, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0560-2020 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 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