Class ITerminated in FDA datasetRecall initiated Jan 6, 2025

My Mochi Sorbet Peach Mango Sorbet; Keep Frozen; 6 pieces per container; 6-1.25 OZ (35g) PIECES…

Recalling firm: The Mochi Ice Cream Company

Why it was recalled

Frozen Peach Mango Sorbet contains undeclared allergen (egg)

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Feb 26, 2025.

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Compare the exact product and package details with the label you have.

ProductMy Mochi Sorbet Peach Mango Sorbet; Keep Frozen; 6 pieces per container; 6-1.25 OZ (35g) PIECES NET WT 7.5 OZ (210g)*** Nutritional Panel: 6 servings per container; JOYFULLY CHILL!; Made in a nut-free facility; Made by My/Mochi, 5563 Alcoa Ave., Los Angeles, CA 90058; www.mymochi.com; Plant No. 06-00024, EU# 3009013677; Product of USA; UPC# 0-70934-99868-1; Affected lots (Lot# 337-24; Lot#341-24)
Package size1.25 OZ
UPC070934998681

FDA code information

USE by: 12/2/2025 and 12/6/2025

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

My Mochi Sorbet Peach Mango Sorbet; Keep Frozen; 6 pieces per container; 6-1.25 OZ (35g) PIECES NET WT 7.5 OZ (210g)*** Nutritional Panel: 6 servings per container; JOYFULLY CHILL!; Made in a nut-free facility; Made by My/Mochi, 5563 Alcoa Ave., Los Angeles, CA 90058; www.mymochi.com; Plant No. 06-00024, EU# 3009013677; Product of USA; UPC# 0-70934-99868-1; Affected lots (Lot# 337-24; Lot#341-24)

Extracted codes and context

TypeCode / valueContext
UPC0709349986810058; www.mymochi.com; Plant No. 06-00024, EU# 3009013677; Product of USA; UPC# 0-70934-99868-1; Affected lots (Lot# 337-24; Lot#341-24)

Original FDA recall reason

Frozen Peach Mango Sorbet contains undeclared allergen (egg)

Recall details

Recall number
F-0431-2025
Event ID
96112
FDA status
Terminated
Initiated
Jan 6, 2025
Reported
Feb 5, 2025
Classified
Jan 28, 2025
Terminated
Feb 26, 2025
Quantity
1350 cases
Location
Vernon, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Product was distributed nationwide. No foreign distribution.

FDA source record · F-0431-2025

Data updated September 16, 2026. View official FDA data ↗

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