Ito En Royal Mills Iced Cappuccino Recall: Sour Taste and Sediment Issues
Ito En recalls Royal Mills Iced Cappuccino (11 fl oz cans) due to sour taste, off odor, and sediment in one lot. Consumers should check UPC 073366 for affected products.
Lower-risk recall
Firm received complaints of sour taste, off odor and sediment in one lot of canned iced Cappuccino.
Contact the company
What happened, in plain English
Ito En is recalling a specific lot of Royal Mills Iced Cappuccino cans because they had sour taste, off odor, and sediment. This issue only affects one lot, so most consumers are not impacted. Read more at govinfonow.com/recall/20524-ito-en-royal-mills-iced-cappuccino-recall-sour-taste-and.
Source Summary by GovInfoNow · govinfonow.com/recall/20524-ito-en-royal-mills-iced-cappuccino-recall-sour-taste-and · Updated October 7, 2026 · FDA enforcement record: FDA #F-2812-2017
Cite this page
“Ito En Royal Mills Iced Cappuccino Recall: Sour Taste and Sediment Issues.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/20524-ito-en-royal-mills-iced-cappuccino-recall-sour-taste-and. Based on FDA recall #F-2812-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2812-2017%22&limit=1).
Why it’s dangerous
The recalled cans had complaints of sour taste, off odor, and sediment. These issues likely came from a problem in the manufacturing process for this specific lot.
Who’s affected
Owners of the recalled 11 fl oz Royal Mills Iced Cappuccino cans with UPC 073366 made in Hawaii are affected. People who bought this specific lot are most at risk.
How to tell if you have this one
Check for the UPC code 073366 on the can. The product was made in Hawaii with a best-by date of June 15, 2018.
- Brand
Ito En- Product
Royal Mills, Iced Cappuccino, Premium Coffee. 11.0 FL. OZ. (325 ml) 2-piece aluminum can; Made in Hawaii. UPC: 0 73366- Category
Food
What to do — step by step
Check Product Details
Look for the UPC code 073366 on the can to confirm if it's the recalled lot.
Where it went and when
Where it was distributed
Distributed in Hawaii.
FDA distribution: “One locations in HI” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Hawaii.
Recall timeline
FDA terminated this recall 3 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-2812-2017 (August 9, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2812-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.