Iberia Codfish Fritter Mix Recalled for Undeclared Soy Allergen
Productos La Finca recalls Iberia Codfish Fritter Mix due to undeclared soy. Check lot numbers and expiration dates if you bought this in Florida.
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Undeclared food allergen: Soy
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What happened, in plain English
Productos La Finca, Inc. is recalling Iberia Codfish Fritter Mix because it contains undeclared soy, which can cause serious allergic reactions in sensitive individuals. The recall affects specific lots distributed only in Florida. No remedy or return instructions are currently listed in the record. Read more at govinfonow.com/recall/23817-iberia-codfish-fritter-mix-recalled-for-undeclared-soy-allergen.
Source Summary by GovInfoNow · govinfonow.com/recall/23817-iberia-codfish-fritter-mix-recalled-for-undeclared-soy-allergen · Updated October 9, 2026 · FDA enforcement record: FDA #F-0347-2017
Cite this page
“Iberia Codfish Fritter Mix Recalled for Undeclared Soy Allergen.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23817-iberia-codfish-fritter-mix-recalled-for-undeclared-soy-allergen. Based on FDA recall #F-0347-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0347-2017%22&limit=1).
Why it’s dangerous
The presence of undeclared soy poses a risk to people with soy allergies or sensitivities. Ingesting the product could trigger an allergic reaction ranging from mild symptoms to severe, life-threatening conditions.
Who’s affected
Consumers in Florida who purchased Iberia Codfish Fritter Mix, particularly those with soy allergies. Individuals who have not yet consumed the product are at risk of an allergic reaction if they do.
How to tell if you have this one
Check your pantry for Iberia Codfish Fritter Mix in boxes containing twelve 4.5 oz pouches. Specifically look for Lot #16076 with an expiration date of 3/16/17, or Lot #16089 with an expiration date of 3/29/17.
- Brand
Iberia- Category
Food
What to do — step by step
Stop consuming the product
Do not eat the Iberia Codfish Fritter Mix if you have soy allergies or if your package matches the recalled lot numbers and expiration dates.
Check lot details
Verify if your product is Lot #16076 (Exp. 3/16/17) or Lot #16089 (Exp. 3/29/17).
Where it went and when
Where it was distributed
Distributed in Florida.
FDA distribution: “USA only: Florida” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Florida.
Recall timeline
FDA terminated this recall 12 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- 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-0347-2017 (July 13, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0347-2017 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.