Mikawaya — FDA Recall History & Enforcement Records
Data Notice: Recall frequency varies by category and firm size; data is comparative and may not indicate actual brand safety or quality. See Methodology.
As of July 22, 2026, Mikawaya has 3 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 9 Jun 2017. Mikawaya is categorized under Dairy based on their predominant recall history.
Recall activity over time for Mikawaya
How serious are Mikawaya recalls?
FDA recall classifications by severity
Full FDA recall history for Mikawaya
All 3 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first
| Date | Product | Reason | Class & Status |
|---|---|---|---|
| 9 Jun 2017Official FDA Notice | Shirakiku Brand Red Bean Ice Cream 3 gallon foodservice tub | Firm is recalling a limited number of Green Tea and Red Bean ice cream due the possibility of the presence of metal fragments. | Class IITerminated |
| 9 Jun 2017Official FDA Notice | Green Tea Ice Cream: Sold under the brand names of: Trader Joe’s Brand Matcha- 1 quart tubs, SKU 055740; Shirakiku br | Firm is recalling a limited number of Green Tea and Red Bean ice cream due the possibility of the presence of metal fragments. | Class IITerminated |
| 9 May 2017Official FDA Notice | Mikawaya Mochi Ice Cream Chocolate Chocolate, 6-1.5oz (43g) pieces, Net Wt. 9.1oz (258g), UPC 070934990609, 24 boxes/cas | Mikawaya is recalling Mochi Ice Cream Chocolate Chocolate because it may contain Chocolate Peanut Butter Ice Cream. | Class ITerminated |
Where have Mikawaya recalls occurred?
States affected across all recorded FDA enforcement actions
Where does this recall data come from?
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Data sourced from the FDA Recall Enterprise System via openFDA API. This information is for educational purposes only and does not constitute health or legal advice. FoodRecallFinder.com is not affiliated with or endorsed by the U.S. Food and Drug Administration.
To determine if your specific product is affected, verify that the brand name, product description, lot number, UPC code, and date range all match the recall details exactly. When in doubt contact the recalling firm or visit FDA.gov.
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