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FDA source record Class I Terminated

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 CHI...

Recall Date: 2025-01-06 Recalling Firm: The Mochi Ice Cream Company Record Ref: F-0431-2025

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns 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 CHI... and names The Mochi Ice Cream Company as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: The Mochi Ice Cream Company
  • Classification: Class I
  • Status: Terminated
  • Recall date: 2025-01-06
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Product Description & Identification

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)

Reason for Recall / Hazard Identified

Frozen Peach Mango Sorbet contains undeclared allergen (egg)

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.

Consumer Action Recorded in the Source

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Distribution & Affected States

Product was distributed nationwide. No foreign distribution.

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
F-0431-2025
Indexed update
2026-08-09 21:59:13 UTC
Official source
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