Class IITerminatedVoluntary: Firm initiated
Gordon Desserts DBA Mochidoki: food recall F-0744-2025
Gordon Desserts DBA Mochidoki of Totowa, NJ recalled Sundae Shoppe, Cookies and Cream Mochi Ice Cream, 6 count, 7.5 oz, Plastic sealed tray inside paper carton. 6 Pieces… Reason: Undeclared Wheat and Soy. The FDA listed it as Class II in its Enforcement Report dated May 7, 2025; distribution: Connecticut, Ohio, Pennsylvania, Virginia.
Record status as published: Terminated (terminated Mar 17, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 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.
- Product quantity
- 5,016 shippers
- Reason for recall
- Undeclared Wheat and Soy
- Codes, lots and dates on the package
- Shipper Lots: 32624,34024,01025, 03125, 05725, 06525, 08025, 08725, 09225
- Distribution pattern
- The recalled product was distributed to the following states: CT, VA, OH and PA
- Recalling firm
- Gordon Desserts DBA Mochidoki, Totowa, NJ
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Apr 3, 2025 |
| Classified by the FDA | Apr 28, 2025 |
| Published in the Enforcement Report | May 7, 2025 |
| Terminated | Mar 17, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0744-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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