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Use caution Food recall · FDA · Published June 30, 2016

El Isleño Sofrito Recalled for Undeclared Yellow #6 Allergen

AC Culinary Group recalls El Isleño Sofrito Gourmet in Puerto Rico due to undeclared FD&C Yellow #6. Check your lot numbers and expiration dates.

🇺🇸 FDA recall #F-1847-2016FoodEl Isleño ›
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Contact the company

Recalling firmAC Culinary Group LLC760 19th St Ste.5 · Catano, PR 00962
✎ GovInfoNow plain-language explainer

What happened, in plain English

AC Culinary Group LLC is recalling El Isleño Sofrito Gourmet Con Sazon Y Achiote because the label does not declare FD&C Yellow #6, a potential allergen. The affected products were sold exclusively in Puerto Rico. Consumers should check their pantry for specific lot numbers and expiration dates to see if they are part of this recall. Read more at govinfonow.com/recall/23908-el-isle-o-sofrito-recalled-for-undeclared-yellow-6-allergen.

Source Summary by GovInfoNow · govinfonow.com/recall/23908-el-isle-o-sofrito-recalled-for-undeclared-yellow-6-allergen · Updated October 9, 2026 · FDA enforcement record: FDA #F-1847-2016

Cite this page

“El Isleño Sofrito Recalled for Undeclared Yellow #6 Allergen.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23908-el-isle-o-sofrito-recalled-for-undeclared-yellow-6-allergen. Based on FDA recall #F-1847-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1847-2016%22&limit=1).

Why it’s dangerous

The product contains FD&C Yellow #6 but fails to list it on the ingredient label. This undeclared allergen poses a risk to individuals who are allergic or sensitive to this dye, as they may unknowingly consume it.

Who’s affected

Consumers in Puerto Rico who purchased El Isleño Sofrito Gourmet Con Sazon Y Achiote, particularly those with sensitivities or allergies to FD&C Yellow #6. The recall affects specific lots distributed within the region.

How to tell if you have this one

Look for El Isleño Sofrito Gourmet Con Sazon Y Achiote in 12 oz or 32 oz packages. Check the label for 'Keep Refrigerated' and 'Hecho en Puerto Rico'. The 12 oz units have LOT 28J with EXP 12/16. The 32 oz units have LOT 31R JN with EXP 09/16.

  • Brand
    El Isleño
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Your Product

    Verify if your package matches the lot numbers (28J for 12oz, 31R JN for 32oz) and expiration dates (12/16 or 09/16).

  2. Contact Manufacturer

    Since the remedy is not stated in the record, contact AC Culinary Group LLC for further instructions on returns or refunds.

Where it went and when

Where it was distributed

Distributed in Puerto Rico.

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: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFLPuerto Rico: yesPR

FDA distribution: “Puerto Rico only.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Puerto Rico.

Recall timeline

FDA terminated this recall 11 months after the firm started it.

1. Firm started the recall: Jun 30, 201612. FDA classified it Class II: Jul 28, 201623. Published in FDA’s Enforcement Report: Aug 3, 201634. FDA terminated the recall: Jun 12, 2017420162017
  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.

✎ GovInfoNow

Questions people ask

Where were these products sold?

The recall distribution pattern is limited to Puerto Rico only.

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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-1847-2016 (June 30, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1847-2016 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 9, 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