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Stop using now Food recall · FDA · Published July 12, 2016

McCain Recalls Anchor Breaded Fiesta Bold Poppers for E. Coli Risk

McCain Foods USA recalls Anchor breaded Fiesta Bold Poppers due to potential E. coli O121 contamination from flour supplied by General Mills.

🇺🇸 FDA recall #F-2097-2016FoodMcCain Foods ›
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Recalling firmMcCain Foods USA2275 Cabot Dr · Lisle, IL 60532-3653
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What happened, in plain English

McCain Foods USA is recalling a specific batch of Anchor breaded Fiesta Bold Poppers because the product may be contaminated with E. coli O121. The contamination originated from flour supplied by General Mills. Consumers should check their freezers for this specific product to avoid potential foodborne illness. Read more at govinfonow.com/recall/23828-mccain-recalls-anchor-breaded-fiesta-bold-poppers-for-e-coli.

Source Summary by GovInfoNow · govinfonow.com/recall/23828-mccain-recalls-anchor-breaded-fiesta-bold-poppers-for-e-coli · Updated October 9, 2026 · FDA enforcement record: FDA #F-2097-2016

Cite this page

“McCain Recalls Anchor Breaded Fiesta Bold Poppers for E. Coli Risk.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23828-mccain-recalls-anchor-breaded-fiesta-bold-poppers-for-e-coli. Based on FDA recall #F-2097-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2097-2016%22&limit=1).

Why it’s dangerous

The product contains flour from General Mills that has been contaminated with E. coli O121. Ingesting this bacteria can cause serious foodborne illness, which is why the recall was issued.

Who’s affected

Consumers who purchased the recalled breaded stuffed jalapenos poppers nationwide are affected. Anyone who has not cooked or discarded the product is at risk of exposure to E. coli O121.

How to tell if you have this one

Look for breaded stuffed jalapenos poppers labeled as "Anchor breaded Fiesta Bold Poppers" or "breaded stuffed jalapenos." The product comes in a green 4 lb. box with white, green, and orange lettering. Check the code "30010718" on the packaging.

  • Brand
    McCain Foods
  • Category
    Food
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    Nationwide. There are no foreign consignees.
Recall numberProduct, codes & lotsQuantity
F-2097-2016Breaded stuffed Jalapenos poppers labeled in part: Anchor breaded Fiesta Bold Poppers, breaded stuffed jalapenos, keep frozen. The product is packaged in a green 4 lb. box with white, green and orange lettering.; 30010718555 cases ( 2, 4 lb. boxes per case)
F-2098-2016Fire roasted Poblano & Jalapeno popper bites packaged in a white box with black lettering. The product is labeled in part: Canchor Poppers Fire Roasted & Jalapeno popper bites, 2-4 lbs.; 300110271, 947 cases (2, 4lb boxes per case)
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the Anchor breaded Fiesta Bold Poppers due to the risk of E. coli contamination.

  2. Discard or return the item

    The recall record does not specify a remedy, so consumers should treat this as a serious hazard and dispose of the product safely.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide. There are no foreign consignees.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 2.8 years after the firm started it.

1. Firm started the recall: Jul 12, 201612. FDA classified it Class II: Sep 8, 201623. Published in FDA’s Enforcement Report: Sep 14, 201634. FDA terminated the recall: Apr 22, 2019420162019
  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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Questions people ask

Where was this product sold?

The recalled product was distributed nationwide in the United States.

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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-2097-2016 (July 12, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2097-2016 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