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Stop using now Food recall · FDA · Published November 14, 2017

Ahold Whole Kernel Sweet Corn Recall: Listeria Risk in Frozen Corn

Ahold recalls frozen whole kernel sweet corn products due to Listeria Monocytogenes detected in retail samples. Consumers should check product labels for affected brands and UPCs.

🇺🇸 FDA recall #F-0421-2018FoodAhold ›
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Contact the company

Recalling firmAhold Usa1385 Hancock St · Quincy, MA 02169-5103
✎ GovInfoNow plain-language explainer

What happened, in plain English

Ahold is recalling frozen whole kernel sweet corn products after testing found Listeria Monocytogenes in some samples. This bacteria can cause serious illness, so affected products should be discarded immediately. Read more at govinfonow.com/recall/20018-ahold-whole-kernel-sweet-corn-recall-listeria-risk-in-frozen.

Source Summary by GovInfoNow · govinfonow.com/recall/20018-ahold-whole-kernel-sweet-corn-recall-listeria-risk-in-frozen · Updated October 7, 2026 · FDA enforcement record: FDA #F-0421-2018

Cite this page

“Ahold Whole Kernel Sweet Corn Recall: Listeria Risk in Frozen Corn.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/20018-ahold-whole-kernel-sweet-corn-recall-listeria-risk-in-frozen. Based on FDA recall #F-0421-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0421-2018%22&limit=1).

Why it’s dangerous

Listeria Monocytogenes is a bacterium that can cause serious infections, especially in pregnant women, newborns, and people with weakened immune systems. The bacteria was detected in retail samples of frozen sweet corn.

Who’s affected

Owners of frozen whole kernel sweet corn products with the described brands and UPCs are affected. Pregnant women, newborns, and others with weakened immune systems are at higher risk.

How to tell if you have this one

Check for products labeled 'Ahold-Own Brands', 'Stop & Shop', 'Giant', or 'GIANT/MARTIN S' with 16 oz. size and UPC 68826700676. Products with 'Best by Oct 2019' and 'B7 276 2' are affected.

  • Brand
    Ahold
  • Product
    Ahold-Own Brands Whole Kernel Sweet Corn, 16 oz. Plastic Bag : Stop & Shop Brand Frozen Whole Kernel Sweet Corn, 16 oz
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop using it now

    Discard all affected frozen whole kernel sweet corn products immediately.

Where it went and when

Where it was distributed

Distributed in 3 states.

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: yesMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: yesPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: yesMDDelaware: 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: “The firm distributed product to the following Direct Accounts: 1). C&S Aberdeen, MD 2). C&S Giant, York, PA 3). C&S Westfield, MA 4). C&S Giant, York, PA 5). C&S Westfield, MA Please see attached excel spread sheet for detail list of…” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Maryland, Massachusetts, Pennsylvania.

Recall timeline

FDA terminated this recall 3.7 years after the firm started it.

1. Firm started the recall: Nov 14, 201712. FDA classified it Class II: Dec 5, 201723. Published in FDA’s Enforcement Report: Dec 6, 201734. FDA terminated the recall: Jul 23, 2021420172021
  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-0421-2018 (November 14, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0421-2018 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