Choice Northwest Recall: cake product is recalled due to undeclared soy lecithin. The canola spray oil containing soy lecithin was used but soy or soy lecithin is not declared on label.

🇺🇸 United States

1. May 5, 2017 - Recall initiated
2. June 14, 2017 - Reported by source
3. August 15, 2017 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-2327-2017

Event ID

77216

Status

Terminated

Classification

Class II

Company

Choice Northwest

Product description

Hazelnut Cake, Paradise Deli brand, net wt. 15 oz., UPC 0 31619 10201 4. The label is read in parts: "***Contains: Oregon grown hazelnuts, cane sugar, organic unbleached wheat flour, fresh eggs, sea salt, pure vanilla***PARADISE DELI - PO Box 22411, Eugene, OR 97402 *** 925 37th Eugene, OR 97405***".

Quantity

36 count

Reason

cake product is recalled due to undeclared soy lecithin. The canola spray oil containing soy lecithin was used but soy or soy lecithin is not declared on label.

Recall initiation date

May 5, 2017

Report date

June 14, 2017

Classification date

Not published in this source record

Termination date

August 15, 2017

Distribution pattern

distributed in Oregon

UPC, lot, and code information

Expiration date 5/13, 5/20

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

Other products recalled under this same event

This recall shares FDA event ID 77216 with 1 other product entry in Public Health Trace.

Responsible company: Choice Northwest

Other recalls from Choice Northwest

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.

• Email
• X / Twitter
• Facebook