My Mochi Strawberry flavored Non-Dairy Frozen Dessert; 7.5 oz; 6 pieces per container. UPC# 0-70934-99645-8
Summary
The FDA issued a Class II for My Mochi Strawberry flavored Non-Dairy Frozen Dessert; 7.5 oz; 6 pieces per cont by The Mochi Ice Cream Company, LLC. Reason: Foreign object found inside retail container..
Details
Source
Food Recall
External ID
H-0684-2026
Action Date
2026-05-06
Status
Terminated
Category
food
Product Description
My Mochi Strawberry flavored Non-Dairy Frozen Dessert; 7.5 oz; 6 pieces per container. UPC# 0-70934-99645-8
Lot/Code Info: Lot# 041-26 BEST BUY 2/20/2027
Quantity Affected: 1270 cases
Reason for Recall
Foreign object found inside retail container.
Distribution
Product was distributed to 6 retail consignees with several locations nationwide.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-04-20
Company
Vernon, CA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 19 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (The Mochi Ice Cream Company, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does The Mochi Ice Cream Company, LLC have FDA actions?
This is the only FDA action we have on record for The Mochi Ice Cream Company, LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0684-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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