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Use caution Food recall · FDA · Published November 20, 2016

GREENCORE Mediterranean Chicken Hummus Sandwich Recall: Listeria Contamination Risk

GREENCORE USA recalls Fresh to Go Mediterranean Chicken Hummus Sandwich due to potential Listeria monocytogenes contamination. Consumers should check use-by dates and avoid consumption.

🇺🇸 FDA recall #F-0686-2017FoodGREENCORE ›
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Recalling firmGREENCORE USA222 Rosewood Dr Ste 240 · Danvers, MA 01923-4520
✎ GovInfoNow plain-language explainer

What happened, in plain English

GREENCORE USA is recalling Fresh to Go Mediterranean Chicken Hummus Sandwiches because they may be contaminated with Listeria monocytogenes. This bacteria can cause serious illness, especially in pregnant women, newborns, and the elderly. Read more at govinfonow.com/recall/22832-greencore-mediterranean-chicken-hummus-sandwich-recall-listeria-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/22832-greencore-mediterranean-chicken-hummus-sandwich-recall-listeria-contamination-risk · Updated October 8, 2026 · FDA enforcement record: FDA #F-0686-2017

Cite this page

“GREENCORE Mediterranean Chicken Hummus Sandwich Recall: Listeria Contamination Risk.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/22832-greencore-mediterranean-chicken-hummus-sandwich-recall-listeria-contamination-risk. Based on FDA recall #F-0686-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0686-2017%22&limit=1).

Why it’s dangerous

Listeria monocytogenes is a bacterium that can cause severe infections in vulnerable populations. The product may be contaminated during the manufacturing process, leading to potential illness if consumed.

Who’s affected

People who purchased the Fresh to Go Mediterranean Chicken Hummus Sandwiches between October 2016 and November 2016 are affected. Pregnant individuals, newborns, and older adults are at higher risk for serious illness from Listeria.

How to tell if you have this one

Check for the Fresh to Go Mediterranean Chicken Hummus Sandwich, packaged in a wedge-shaped plastic container, with a net weight of 8 oz (227g). The product was sold from October 2016 through November 2016.

  • Brand
    GREENCORE
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Dates

    Look for use-by dates on the packaging, which range from October 17, 2016 to November 21, 2016.

  2. Discard Unsafe Product

    If the product is within the use-by dates, discard it immediately to avoid potential illness.

Where it went and when

Where it was distributed

Distributed in 11 states.

Alaska: not listedAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: yesWIMichigan: not listedMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: yesIAIndiana: yesINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: yesCTCalifornia: 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 listedFL

FDA distribution: “Illinois, Indiana, Iowa, Wisconsin and Massachusetts, Rhode Island, Connecticut, maine, Vermont, New Hampshire and New York” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Connecticut, Illinois, Indiana, Iowa, Maine, Massachusetts, New Hampshire, New York, Rhode Island, Vermont, Wisconsin.

Recall timeline

FDA terminated this recall 38 days after the firm started it.

1. Firm started the recall: Nov 20, 201612. FDA classified it Class I: Dec 9, 201623. Published in FDA’s Enforcement Report: Dec 21, 201634. FDA terminated the recall: Dec 28, 201642016
  1. Firm started the recall
  2. FDA classified it Class I
  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-0686-2017 (November 20, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0686-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 8, 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