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Stop using now Food recall · FDA · Published June 2, 2016

Five Star Gourmet Foods Recalls Energizer Box Due to Listeria Risk

Five Star Gourmet Foods recalls Energizer Box items due to potential Listeria monocytogenes contamination. Check lot numbers and item code FG10144.

🇺🇸 FDA recall #F-0684-2017FoodFive Star Gourmet Foods ›
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Recalling firmFive Star Gourmet Foods, Inc.3880 Ebony St · Ontario, CA 91761-1500
✎ GovInfoNow plain-language explainer

What happened, in plain English

Five Star Gourmet Foods, Inc. is recalling its Energizer Box product because it may be contaminated with Listeria monocytogenes. The recall covers approximately 9,186 cases distributed in California. The company has not yet provided a specific remedy or return instructions in this record. Read more at govinfonow.com/recall/24177-five-star-gourmet-foods-recalls-energizer-box-due-to-listeria.

Source Summary by GovInfoNow · govinfonow.com/recall/24177-five-star-gourmet-foods-recalls-energizer-box-due-to-listeria · Updated October 9, 2026 · FDA enforcement record: FDA #F-0684-2017

Cite this page

“Five Star Gourmet Foods Recalls Energizer Box Due to Listeria Risk.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/24177-five-star-gourmet-foods-recalls-energizer-box-due-to-listeria. Based on FDA recall #F-0684-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0684-2017%22&limit=1).

Why it’s dangerous

Listeria monocytogenes is a bacteria that can cause serious infections in humans. Infection can lead to fever, muscle aches, and gastrointestinal symptoms, and may spread to the nervous system causing meningitis or septicemia.

Who’s affected

Consumers in California who purchased the Energizer Box with Item Code FG10144 and one of the listed lot numbers are affected. Individuals with weakened immune systems, pregnant women, older adults, and newborns are at highest risk for serious infection from Listeria.

How to tell if you have this one

Check your product for Item Code FG10144. Verify if the lot number matches one of the following: 11216, 11116, 11316, 11716, 11916, 12016, 12416, 12616, 12716, or 12516. The product was distributed to consumers in California.

  • Brand
    Five Star Gourmet Foods
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the Energizer Box if it matches the recalled item code and lot numbers due to Listeria risk.

  2. Check your lot numbers

    Compare the lot number on your package against the list: 11216, 11116, 11316, 11716, 11916, 12016, 12416, 12616, 12716, and 12516.

  3. Monitor for symptoms

    If you have consumed the product and experience fever, muscle aches, or gastrointestinal issues, contact your healthcare provider immediately.

Where it went and when

Where it was distributed

Distributed in California.

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: yesCAUtah: 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: “U.S. distribution to the following; CA. No foregin distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California.

Recall timeline

FDA terminated this recall 7 months after the firm started it.

1. Firm started the recall: Jun 2, 201612. FDA classified it Class I: Dec 9, 201623. Published in FDA’s Enforcement Report: Dec 21, 201634. FDA terminated the recall: Dec 21, 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-0684-2017 (June 2, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0684-2017 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.
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