FDA recall record

Ikko International Trading Wheat Cake recall — FDA F-0004-2015

This voluntary recall has been initiated because Maruto 'C' Cakes (Wheat Cakes) omitted soy lecithin as an ingredient and an accompanying allergen warning.

Class IIclassification
F-0004-2015official record ID
Oct 15, 2014report date

Recall record at a glance

Official recordF-0004-2015
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmIkko International Trading LLC
Report dateOct 15, 2014
Recall initiation dateAug 5, 2014
Quantity10 cases (160 pieces)
LocationElizabeth, NJ, United States

Official product description

Wheat Cake (Maruto "C" Cake), 6.3 ounces (180g), individually packaged in gold foil pouches and sold under the Maruto Brand. Sold at retail locations in display cases containing 8 bars per display case.

Why the product was recalled

This voluntary recall has been initiated because Maruto 'C' Cakes (Wheat Cakes) omitted soy lecithin as an ingredient and an accompanying allergen warning.

Distribution information

US: Illinois

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: Letter.

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.