Ito En (USA) Inc. Recall: Firm received complaints of sour taste, off odor and sediment in one lot of canned iced Cappuccino.
United States
TerminatedClass II
- Company
- Ito En (USA) Inc.
- Product
- Royal Mills, Iced Cappuccino, Premium Coffee. 11.0 FL. OZ.…
- Recall date
- August 9, 2017
- Terminated
- October 25, 2017
- Source
- FDA
Reason for recall
Firm received complaints of sour taste, off odor and sediment in one lot of canned iced Cappuccino.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Royal Mills, Iced Cappuccino, Premium Coffee. 11.0 FL. OZ. (325 ml) 2-piece aluminum can; Made in Hawaii. UPC: 0 73366 12755 | Not published in this source record | 38 cases (6 x 4 packs) | IHJUN15181452 ~ 1456 (Best By Code: ITO EN Hawaii JUN 15 2018, military time); P061517CAP - (Production Code: Production 06 1517 CAPpuccino) |
Distribution
- One locations in HI
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-2812-2017
- Event ID
- 77942
- Status
- Terminated
- Classification
- Class II
- Company
- Ito En (USA) Inc.
- Product description
- Royal Mills, Iced Cappuccino, Premium Coffee. 11.0 FL. OZ. (325 ml) 2-piece aluminum can; Made in Hawaii. UPC: 0 73366 12755
- Quantity
- 38 cases (6 x 4 packs)
- Reason
- Firm received complaints of sour taste, off odor and sediment in one lot of canned iced Cappuccino.
- Recall initiation date
- August 9, 2017
- Report date
- August 30, 2017
- Classification date
- Not published in this source record
- Termination date
- October 25, 2017
- Distribution pattern
- One locations in HI
- UPC, lot, and code information
- IHJUN15181452 ~ 1456 (Best By Code: ITO EN Hawaii JUN 15 2018, military time); P061517CAP - (Production Code: Production 06 1517 CAPpuccino)
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Telephone
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Ito En (USA) Inc.
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Hawaii | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
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