FDA recall record

Chuckanut Bay Foods Item 38180-12, Chuckanut Bay Cheesecake Bites New York + recall — FDA F-1436-2022

Undeclared Soy Lecithin. Label declares Chocolate Compound (Sunflower Lecithin) instead of Soy Lecithin.

Class IIclassification
F-1436-2022official record ID
Jul 27, 2022report date

Recall record at a glance

Official recordF-1436-2022
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmChuckanut Bay Foods LLC
Report dateJul 27, 2022
Recall initiation dateJul 6, 2022
Quantity2,686 cases
LocationBlaine, WA, United States

Official product description

Item 38180-12, Chuckanut Bay Cheesecake Bites New York + Chocolate. Perishable - Keep Refrigerated. There are 8 pieces per plastic clamshell pack and 12 packs per case. Net wt. per pack 6.4 oz. UPC 6 03812 38180 2. The label is read in parts: "***INGREDIENTS: CREAM CHEESE***, CHOCOLATE COMPOUND (sunflower lecithin***), CANE SUGAR, PASTEURIZED CULTURED MILK & CREAM, EGGS, SOUR CREAM, BUTTER OIL, ENRICHED FLOUR (wheat flour***), COCOA, SALT, CAROB BEAN GUM, GUAR GUM, NATURAL FLAVOR, VANILLA EXTRACT. CONTAINS: Eggs, Milk, Wheat***".

Why the product was recalled

Undeclared Soy Lecithin. Label declares Chocolate Compound (Sunflower Lecithin) instead of Soy Lecithin.

Distribution information

Distributed in AL, CA, CO, FL, IL, MA, MI, MN, NY, OR, TX, WA, and WI.

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.