New Seasons Market LLC Recall: 9 inch Asparagus and Goat Cheese Quiche is recalled because egg is declared in the Ingredients statement but it is not declared in the Contains statement.

🇺🇸 United States

1. March 5, 2018 - Recall initiated
2. March 21, 2018 - Reported by source
3. March 16, 2018 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0916-2018

Event ID

79440

Status

Terminated

Classification

Class II

Company

New Seasons Market LLC

Product description

9 inch Asparagus and Goat Cheese Quiche, packaged in a cardboard box with a clear window. UPC # 2 52209 10599 8. The retail label is read in parts: "***ASPARAGUS GOAT CHEESE QUICHE ***NEW SEASONS MARKET***Egg, whole milk, fresh goat cheese, sour cream (milk, cream, nonfat dry milk, enzyme), asparagus, salt, pie shell (wheat flour, canola oil, modified palm oil shortening, water, cornstarch, corn flour, dextrose, salt, soy lecithin, protease enzyme, sodium propionate)***Contains: WHEAT, SOY, MILK.

Quantity

45 units

Reason

9 inch Asparagus and Goat Cheese Quiche is recalled because egg is declared in the Ingredients statement but it is not declared in the Contains statement.

Recall initiation date

March 5, 2018

Report date

March 21, 2018

Classification date

Not published in this source record

Termination date

March 16, 2018

Distribution pattern

distributed in Oregon and Washington

UPC, lot, and code information

Packed on Mar 04,18; Sell By Mar 09, 18

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: New Seasons Market LLC

Other recalls from New Seasons Market LLC

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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