FDA recall record

Chuckanut Bay Foods Red Velvet Layered Cheesecake is one whole cake recall — FDA F-1029-2020

Undeclared walnut. Carrot Cake Layered Cheesecake was incorrectly decorated as Red Velvet Layered Cheesecake and was mis-labeled. Finished product label…

Class IIclassification
F-1029-2020official record ID
Jul 29, 2020report date

Recall record at a glance

Official recordF-1029-2020
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmChuckanut Bay Foods LLC
Report dateJul 29, 2020
Recall initiation dateJun 25, 2020
Quantity60 cakes
LocationBlaine, WA, United States

Official product description

Red Velvet Layered Cheesecake is one whole cake (9" round cake) that has been pre-sliced into 14 slices and packaged in a white case box. Cheesecake is wrapped in a white band, ran through a shrink wrap machine and then put in a white case pack. Net weight: 82 oz. UPC 603812924900. Product must be stored frozen until use or refrigerated for up to 10 days. The cake is frosted with cream cheese frosting, coated in red velvet crumbs and then topped with White Chocolate Blossoms. The recalled cakes were frosted and decorated with red velvet crumbs and it appears as red velvet layered cheesecake on the outside, but the actual cake inside is carrot cake layers cheesecake. Upon opening up the cake walnut pieces would be visible and layers are distinguishable between the carrot and red velvet.

Why the product was recalled

Undeclared walnut. Carrot Cake Layered Cheesecake was incorrectly decorated as Red Velvet Layered Cheesecake and was mis-labeled. Finished product label does not declare walnut.

Distribution information

distribute in CA

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.