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Use caution Food recall · FDA · Published March 5, 2018

New Seasons Market Quiche Recall: Undeclared Egg Allergen

New Seasons Market recalls 9-inch Asparagus and Goat Cheese Quiche due to undeclared egg. Check your UPC and expiration date for details.

🇺🇸 FDA recall #F-0916-2018FoodNew Seasons Market ›
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Contact the company

Recalling firmNew Seasons Market LLC1300 Se Stark St Ste 401 · Portland, OR 97214-2473
✎ GovInfoNow plain-language explainer

What happened, in plain English

New Seasons Market LLC is recalling 45 units of its 9-inch Asparagus and Goat Cheese Quiche because the product contains egg, which is not listed in the 'Contains' statement on the label. This mislabeling poses a risk to individuals with egg allergies who might consume the product unknowingly. The quiche was distributed in Oregon and Washington. Read more at govinfonow.com/recall/19602-new-seasons-market-quiche-recall-undeclared-egg-allergen.

Source Summary by GovInfoNow · govinfonow.com/recall/19602-new-seasons-market-quiche-recall-undeclared-egg-allergen · Updated October 11, 2026 · FDA enforcement record: FDA #F-0916-2018

Cite this page

“New Seasons Market Quiche Recall: Undeclared Egg Allergen.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/19602-new-seasons-market-quiche-recall-undeclared-egg-allergen. Based on FDA recall #F-0916-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0916-2018%22&limit=1).

Why it’s dangerous

The hazard arises because the product contains egg, but the label fails to declare it in the 'Contains' section. This omission can lead to accidental ingestion by people who avoid eggs due to allergies, potentially causing a serious allergic reaction.

Who’s affected

Consumers in Oregon and Washington who purchased the recalled quiche are affected. Individuals with egg allergies are at the highest risk of an allergic reaction due to the undeclared ingredient.

How to tell if you have this one

Check for a cardboard box with a clear window containing a 9-inch Asparagus and Goat Cheese Quiche. Look for UPC # 2 52209 10599 8 on the label. Verify the 'Packed on' date of Mar 04, 18, and the 'Sell By' date of Mar 09, 18.

  • Brand
    New Seasons Market
  • Product
    9 inch Asparagus and Goat Cheese Quiche, packaged in a cardboard box with a clear window. UPC # 2 52209 10599 8. The
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Your Product

    Verify if you have the 9-inch Asparagus and Goat Cheese Quiche with UPC # 2 52209 10599 8 and a Sell By date of Mar 09, 18.

  2. Do Not Consume

    If you have the recalled product, do not eat it due to the undeclared egg allergen.

Where it went and when

Where it was distributed

Distributed in Oregon and Washington.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: 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 Oregon and Washington” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Oregon, Washington.

Recall timeline

FDA terminated this recall 11 days after the firm started it.

1. Firm started the recall: Mar 5, 201812. FDA classified it Class II: Mar 13, 201823. FDA terminated the recall: Mar 16, 201834. Published in FDA’s Enforcement Report: Mar 21, 201842018
  1. Firm started the recall
  2. FDA classified it Class II
  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.

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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-0916-2018 (March 5, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0916-2018 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