CLASS II Food recall · Reported 30 Aug 2017 · FDA Enforcement Report
Royal Mills, Iced Cappuccino, Premium Coffee recalled by Ito En (USA)
Ito En is recalling Royal Mills, Iced Cappuccino, Premium Coffee, distributed in Hawaii. The recall was initiated on 9 Aug 2017 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-2812-2017
- FDA event ID
- 77942
- Recalling firm
- Ito En, Honolulu, HI
- Brand
- Royal Mills
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 9 Aug 2017
- FDA classified
- 18 Aug 2017
- Reported
- 30 Aug 2017
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Other Reasons
- Product category
- Coffee
Timeline
| 9 Aug 2017 | Recall initiated by company | |
| 18 Aug 2017 | Classified by FDA | +9 days |
| 30 Aug 2017 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Firm received complaints of sour taste, off odor and sediment in one lot of canned iced Cappuccino.
Product as listed by the FDA
Royal Mills, Iced Cappuccino, Premium Coffee. 11.0 FL. OZ. (325 ml) 2-piece aluminum can; Made in Hawaii. UPC: 0 73366 12755
Where it was distributed
One locations in HI
Questions about this recall
Why was it recalled?
Firm received complaints of sour taste, off odor and sediment in one lot of canned iced Cappuccino.
Which lots are affected?
IHJUN15181452 ~ 1456 (Best By Code: ITO EN Hawaii JUN 15 2018, military time); P061517CAP - (Production Code: Production 06 1517 CAPpuccino)
Where was it sold?
One locations in HI
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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