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Lower risk Food recall · FDA · Published March 15, 2018

All American Seasonings Lost Cajun Gumbo Base Recall: Salmonella Contamination Risk

All American Seasonings recalls 45lb Lost Cajun Gumbo Base (Lot 80681, Feb 2018) due to Salmonella contamination. Consumers should avoid using this product to prevent foodborne illness.

🇺🇸 FDA recall #F-1008-2018FoodAll American Seasonings ›
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Contact the company

Recalling firmAll American Seasonings, Inc.10600 E 54th Ave · Denver, CO 80239-2145
✎ GovInfoNow plain-language explainer

What happened, in plain English

All American Seasonings is recalling their Lost Cajun Gumbo Base (45lb bags) because it was contaminated with Salmonella. This poses a risk of foodborne illness if the product is used in cooking or eating. Read more at govinfonow.com/recall/19554-all-american-seasonings-lost-cajun-gumbo-base-recall-salmonella-contamination.

Source Summary by GovInfoNow · govinfonow.com/recall/19554-all-american-seasonings-lost-cajun-gumbo-base-recall-salmonella-contamination · Updated October 7, 2026 · FDA enforcement record: FDA #F-1008-2018

Cite this page

“All American Seasonings Lost Cajun Gumbo Base Recall: Salmonella Contamination Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19554-all-american-seasonings-lost-cajun-gumbo-base-recall-salmonella-contamination. Based on FDA recall #F-1008-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1008-2018%22&limit=1).

Why it’s dangerous

Salmonella is a bacteria that can cause food poisoning. If the contaminated product is eaten, it may lead to symptoms like diarrhea, fever, and stomach cramps. The risk is low for most people but can be serious for vulnerable groups like young children, elderly, or those with weakened immune systems.

Who’s affected

Anyone who purchased or uses the recalled Lost Cajun Gumbo Base (45lb bags) from All American Seasonings. People most at risk are those who have cooked or consumed the product.

How to tell if you have this one

Check for 45lb bags labeled 'Lost Cajun Gumbo Base, T4014' with lot number 80681, manufactured on February 22, 2018. The product was sold at units B & C in Denver, CO.

  • Brand
    All American Seasonings
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the lot number 80681 and manufacture date of February 22, 2018 on the packaging.

Where it went and when

Where it was distributed

Distributed in Colorado.

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: yesCONebraska: 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 listedFL

FDA distribution: “One customer in Colorado.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Colorado.

Recall timeline

FDA terminated this recall 3 months after the firm started it.

1. Firm started the recall: Mar 15, 201812. FDA classified it Class II: Apr 11, 201823. Published in FDA’s Enforcement Report: Apr 18, 201834. FDA terminated the recall: Jun 27, 201842018
  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-1008-2018 (March 15, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1008-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 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