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Class IITerminated in FDA datasetRecall initiated May 5, 2017

Hazelnut Cake, Paradise Deli brand, net wt. 15 oz.

Recalling firm: Choice Northwest

Why it was recalled

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.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Aug 15, 2017.

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Compare the exact product and package details with the label you have.

ProductHazelnut 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***".
Package size15 oz
UPC031619102014

FDA code information

Expiration date 5/13, 5/20

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Full FDA record and distribution details

Original 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***".

Extracted codes and context

TypeCode / valueContext
UPC031619102014Hazelnut 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

Original FDA recall 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 details

Recall number
F-2327-2017
Event ID
77216
FDA status
Terminated
Initiated
May 5, 2017
Reported
Jun 14, 2017
Classified
Jun 5, 2017
Terminated
Aug 15, 2017
Quantity
36 count
Location
Eugene, OR, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

distributed in Oregon

FDA source record · F-2327-2017

Data updated September 16, 2026. View official FDA data ↗

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