New Seasons Market LLC Recall: Honey Cake's sticker on the top of a package states "buttermilk and sour cream" but milk is not declared. The bottom scale label has the Contains statement but "MILK" is not declared.

🇺🇸 United States

1. September 27, 2019 - Recall initiated
2. November 6, 2019 - Reported by source
3. October 25, 2019 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0075-2020

Event ID

83912

Status

Terminated

Classification

Class II

Company

New Seasons Market LLC

Product description

Honey Cake, internal PLU code 203190, is a seasonal bakery product. A loaf shaped cake is wrapped with cellophane, stored ambient, and sold from displayed tables. The orange sticker on top of the package is read in parts: "***SEASONAL HONEY CAKE ***Made in small batches, with Bee Local Willamette Valley Honey, Stumptown Coffee, Local Cage-Free Eggs, Local Buttermilk & Sour Cream***". The scale white label at the bottom of the package is read in parts: "***Flour, eggs, honey, sugar, canola oil, coffee, raisins, baking soda, salt, cinnamon, baking powder, ginger*** Contains: eggs, wheat***".

Quantity

535 units.

Reason

Honey Cake's sticker on the top of a package states "buttermilk and sour cream" but milk is not declared. The bottom scale label has the Contains statement but "MILK" is not declared.

Recall initiation date

September 27, 2019

Report date

November 6, 2019

Classification date

Not published in this source record

Termination date

October 25, 2019

Distribution pattern

distributed in Oregon and Washington

UPC, lot, and code information

best by up to and including 9/29/19

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

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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