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Use caution Food recall · FDA · Published December 9, 2015

Eaton Farm Peanut Butter Lust Bar Recall: Undeclared Soy Allergen

Eaton Farm Confectionaries recalls Peanut Butter Lust Bars due to undeclared soy lecithin. Check your UPC and dispose of the product if affected.

🇺🇸 FDA recall #F-0513-2016FoodEaton Farm Confectionaries ›
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Contact the company

Recalling firmEaton Farm Confectionaries, Inc.30 Burbank Rd · Sutton, MA 01590-2426
✎ GovInfoNow plain-language explainer

What happened, in plain English

Eaton Farm Confectionaries, Inc. is recalling Peanut Butter Lust Bars because the packaging fails to list soy lecithin as an ingredient. This omission poses a risk to individuals with soy allergies who may unknowingly consume the allergen. The recall affects fewer than 800 bars distributed in Massachusetts, Maine, Vermont, and New Hampshire. Read more at govinfonow.com/recall/25608-eaton-farm-peanut-butter-lust-bar-recall-undeclared-soy-allergen.

Source Summary by GovInfoNow · govinfonow.com/recall/25608-eaton-farm-peanut-butter-lust-bar-recall-undeclared-soy-allergen · Updated October 11, 2026 · FDA enforcement record: FDA #F-0513-2016

Cite this page

“Eaton Farm Peanut Butter Lust Bar Recall: Undeclared Soy Allergen.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/25608-eaton-farm-peanut-butter-lust-bar-recall-undeclared-soy-allergen. Based on FDA recall #F-0513-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0513-2016%22&limit=1).

Why it’s dangerous

The product contains soy lecithin, but the packaging only states 'Lecithin' without specifying it is derived from soy. This can cause an allergic reaction in people who are sensitive to or allergic to soy products.

Who’s affected

Consumers who purchased Peanut Butter Lust Bars in Massachusetts, Maine, Vermont, or New Hampshire are affected. Individuals with soy allergies are at the highest risk due to the undeclared allergen.

How to tell if you have this one

Look for Peanut Butter Lust Bars with a net weight of 2 ounces and UPC code 1425361001. There is no lot number associated with this recall. The product was sold in Massachusetts, Maine, Vermont, and New Hampshire.

  • Brand
    Eaton Farm Confectionaries
  • Product
    Peanut Butter Lust Bar, Net weight 2 ounces, UPC: 1425361001
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Your Product

    Verify if you have a Peanut Butter Lust Bar with UPC 1425361001.

  2. Avoid Consumption

    Do not eat the product if you have a soy allergy due to the undeclared ingredient.

Where it went and when

Where it was distributed

Distributed in 4 states.

Alaska: not listedAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: 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: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: 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: “Massachusetts, Maine, Vermont & New Hampshire” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Maine, Massachusetts, New Hampshire, Vermont.

Recall timeline

FDA terminated this recall 3.6 years after the firm started it.

1. Firm started the recall: Dec 9, 201512. FDA classified it Class II: Jan 18, 201623. Published in FDA’s Enforcement Report: Jan 27, 201634. FDA terminated the recall: Jul 18, 2019420152019
  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-0513-2016 (December 9, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0513-2016 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 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