FDA recall record

Amlag & Quibuyen, LLC dba Hood Famous Bake Shop Ube recall — FDA F-0354-2023

Ube cheesecake is recalled because Coconut is declared in the ingredients statement, but Coconut is not declared in the Contains statement.

Class IIclassification
F-0354-2023official record ID
Feb 22, 2023report date

Recall record at a glance

Official recordF-0354-2023
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmAmlag & Quibuyen, LLC dba Hood Famous Bake Shop
Report dateFeb 22, 2023
Recall initiation dateJan 25, 2023
Quantity10/2 lbs. units and 109/4oz. units
LocationSeattle, WA, United States

Official product description

Ube (Purple Yam) Cheesecake Coconut Butter Biscuit Crust (4oz) - UPC 6 60845 37067 8. Ube (Purple Yam) Cheesecake Coconut Butter Biscuit Crust (2 lbs.) - UPC 6 60845 37068 5

Why the product was recalled

Ube cheesecake is recalled because Coconut is declared in the ingredients statement, but Coconut is not declared in the Contains statement.

Distribution information

Distributed in WA.

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: E-Mail.

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.