Class IITerminatedVoluntary: Firm initiated
The Mochi Ice Cream Company, LLC: food recall H-0684-2026
The Mochi Ice Cream Company, LLC of Vernon, CA recalled My Mochi Strawberry flavored Non-Dairy Frozen Dessert; 7.5 oz; 6 pieces per container. UPC# 0-70934-99645-8. Reason: Foreign object found inside retail container. The FDA listed it as Class II in its Enforcement Report dated May 6, 2026; distribution: nationwide.
Record status as published: Terminated (terminated May 19, 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
- My Mochi Strawberry flavored Non-Dairy Frozen Dessert; 7.5 oz; 6 pieces per container. UPC# 0-70934-99645-8
- Product quantity
- 1270 cases
- Reason for recall
- Foreign object found inside retail container.
- Codes, lots and dates on the package
- Lot# 041-26 BEST BUY 2/20/2027
- Distribution pattern
- Product was distributed to 6 retail consignees with several locations nationwide.
- Recalling firm
- The Mochi Ice Cream Company, LLC, Vernon, CA
- 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
- Telephone
Advertisement
Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Apr 20, 2026 |
| Classified by the FDA | Apr 30, 2026 |
| Published in the Enforcement Report | May 6, 2026 |
| Terminated | May 19, 2026 |
Advertisement
OpenPlate shows FDA records as published and does not add new findings. Product names and company names belong to their owners.
Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0684-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.