FDA recall record

Gordon Desserts DBA Mochidoki Sundae Shoppe, Cookies and Cream Mochi Ice Cream, 6 count, 7.5 recall — FDA F-0744-2025

Undeclared Wheat and Soy

Class IIclassification
F-0744-2025official record ID
May 7, 2025report date

Recall record at a glance

Official recordF-0744-2025
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmGordon Desserts DBA Mochidoki
Report dateMay 7, 2025
Recall initiation dateApr 3, 2025
Quantity5,016 shippers
LocationTotowa, NJ, United States

Official product description

Sundae Shoppe, Cookies and Cream Mochi Ice Cream, 6 count, 7.5 oz, Plastic sealed tray inside paper carton. 6 Pieces per carton, 8 cartons per shipper. Keep frozen.

Why the product was recalled

Undeclared Wheat and Soy

Distribution information

The recalled product was distributed to the following states: CT, VA, OH and PA

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.