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Lower risk Food recall · FDA · Published April 30, 2018

Stonewall Kitchen Basil Pesto Aioli Recall: Undeclared Eggs in Product

Stonewall Kitchen recalls 10.25 oz Basil Pesto Aioli due to possible undeclared eggs. Consumers should check labels for correct net weight and enjoy by date.

🇺🇸 FDA recall #F-1440-2018FoodStonewall Kitchen ›
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Recalling firmStonewall Kitchen, LLC2 Stonewall Ln · York, ME 03909-1662
✎ GovInfoNow plain-language explainer

What happened, in plain English

Stonewall Kitchen is recalling Basil Pesto Aioli that may contain undeclared eggs. This could pose a risk for people with egg allergies. The product was sold with incorrect labeling. Read more at govinfonow.com/recall/19153-stonewall-kitchen-basil-pesto-aioli-recall-undeclared-eggs-in-product.

Source Summary by GovInfoNow · govinfonow.com/recall/19153-stonewall-kitchen-basil-pesto-aioli-recall-undeclared-eggs-in-product · Updated October 7, 2026 · FDA enforcement record: FDA #F-1440-2018

Cite this page

“Stonewall Kitchen Basil Pesto Aioli Recall: Undeclared Eggs in Product.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19153-stonewall-kitchen-basil-pesto-aioli-recall-undeclared-eggs-in-product. Based on FDA recall #F-1440-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1440-2018%22&limit=1).

Why it’s dangerous

The product may contain undeclared eggs, which could cause allergic reactions in people sensitive to eggs. The product was incorrectly labeled as Basil Pesto (8 oz) instead of the actual 10.25 oz size.

Who’s affected

People who purchased Stonewall Kitchen Basil Pesto Aioli with a net weight of 10.25 oz. and UPC 7 11381 03060 8 are affected. Those with egg allergies are at higher risk.

How to tell if you have this one

Check for the product label stating 'Basil Pesto Aioli Net Weight 10.25 oz' with UPC 7 11381 03060 8. The product was sold with an incorrect label showing net weight 8 oz instead of 10.25 oz.

  • Brand
    Stonewall Kitchen
  • Product
    STONEWALL KITCHEN Basil Pesto Aioli Net Weight Net 10.25 oz. UPC: 7 11381 03060 8. Product is incorrectly labeled as
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Label

    Look for the product label that states 'Basil Pesto Aioli Net Weight 10.25 oz' with UPC 7 11381 03060 8.

Where it went and when

Where it was distributed

Distributed in 21 states.

Alaska: yesAKMaine: not listedMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: yesMAOregon: not listedORNevada: not listedNVWyoming: yesWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: not listedUTColorado: yesCONebraska: not listedNEMissouri: yesMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: yesAZNew Mexico: not listedNMKansas: not listedKSArkansas: yesARTennessee: not listedTNNorth Carolina: yesNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: yesTXFlorida: yesFL

FDA distribution: “AK, AR, AZ, CA, CO, CT, FL, IL, MA, MN, MO, NC, NH, NJ, NY, PA, TX, VT, WA, WI, WY” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Florida, Illinois, Massachusetts, Minnesota, Missouri, New Hampshire, New Jersey, New York, North Carolina, Pennsylvania, Texas, Vermont, Washington, Wisconsin, Wyoming.

Recall timeline

FDA terminated this recall 57 days after the firm started it.

1. Firm started the recall: Apr 30, 201812. FDA classified it Class I: May 11, 201823. Published in FDA’s Enforcement Report: May 16, 201834. FDA terminated the recall: Jun 26, 201842018
  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-1440-2018 (April 30, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1440-2018 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