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Lower risk Food recall · FDA · Published February 20, 2018

Market of Choice Sezam Kale Salad Kits Recall: Undeclared Egg in Dressing

Market of Choice recalls Sezam Kale Salad ingredient kits (6.43 lbs) due to undeclared egg in dressing. Products sold with UPC 2 11565 20216 1 and production codes 02-14-18 or 02-15-18.

🇺🇸 FDA recall #F-0878-2018FoodMarket of Choice ›
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Recalling firmMarket of Choice Inc1150 Owen Loop S · Eugene, OR 97402-9199
✎ GovInfoNow plain-language explainer

What happened, in plain English

Market of Choice is recalling Sezam Kale Salad ingredient kits that contain undeclared egg in the dressing. This poses a risk for people with egg allergies as the dressing may cause an allergic reaction. Read more at govinfonow.com/recall/19644-market-of-choice-sezam-kale-salad-kits-recall-undeclared-egg.

Source Summary by GovInfoNow · govinfonow.com/recall/19644-market-of-choice-sezam-kale-salad-kits-recall-undeclared-egg · Updated October 7, 2026 · FDA enforcement record: FDA #F-0878-2018

Cite this page

“Market of Choice Sezam Kale Salad Kits Recall: Undeclared Egg in Dressing.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19644-market-of-choice-sezam-kale-salad-kits-recall-undeclared-egg. Based on FDA recall #F-0878-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0878-2018%22&limit=1).

Why it’s dangerous

The dressing packet in the kit contains undeclared egg, which can cause allergic reactions in people sensitive to egg. The product was sold in deli cases at retail stores with specific production dates.

Who’s affected

People who purchased the Sezam Kale Salad ingredient kits with UPC 2 11565 20216 1 between February 14-15, 2018. Those with egg allergies are most at risk.

How to tell if you have this one

Check for the UPC 2 11565 20216 1 on the product. Products with production codes 02-14-18 (sell by 02-21-18) or 02-15-18 (sell by 02-22-18) are affected.

  • Brand
    Market of Choice
  • Product
    Sezam Kale Salad ingredient kits, net wt. 6.43 pound. Ingredients are packaged individually and then placed in one
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the UPC 2 11565 20216 1 and production codes 02-14-18 or 02-15-18 on the kit.

Where it went and when

Where it was distributed

Distributed in Oregon.

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: yesORNevada: 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: “distributed in OR” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Oregon.

Recall timeline

FDA terminated this recall 13 days after the firm started it.

1. Firm started the recall: Feb 20, 201812. FDA classified it Class I: Mar 1, 201823. FDA terminated the recall: Mar 5, 201834. Published in FDA’s Enforcement Report: Mar 7, 201842018
  1. Firm started the recall
  2. FDA classified it Class I
  3. FDA terminated the recall
  4. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

Is there a risk of serious injury?

No, the recall is for people with egg allergies. There is no risk of serious injury from this product.

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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-0878-2018 (February 20, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0878-2018 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