FDMR, INC DBA SUJI'S KOREAN CUISINE Recall: Hazelnuts were declared in ingredient statement but not in Contains statement.
United States
TerminatedClass II
- Company
- FDMR, INC DBA SUJI'S KOREAN CUISINE
- Product
- Taiyaki Variety Pack; 21.6 oz. (600g) 30 fish waffles in a…
- Recall date
- February 17, 2022
- Terminated
- July 6, 2022
- Source
- FDA
Reason for recall
Hazelnuts were declared in ingredient statement but not in Contains statement.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Taiyaki Variety Pack; 21.6 oz. (600g) 30 fish waffles in a units, 27 master cased to a pallet, 40 pallets to container. Item Number 1598329, UPC: 8 50013 07258 3 Three flavors: Chocolate Cream, Vanilla Custard and Red Bean & Cinnamon. Manufactured for Suji's Korean Cuisine, Seattle, WA Country of Origin: Republic of Korea. | Not published in this source record | 63,451sold | All lots |
Distribution
- Nationwide to wholesale customer locations in AK
- AL
- AR
- AZ
- CA
- CO
- CT
- DC
- DE
- FL
- GA
- HI
- IA
- ID
- IL
- IN
- KS
- KY
- LA
- MA
- MD
- MI
- MN
- MO
- MS
- MT
- NA
- NC
- ND
- NE
- NH
- NJ
- NM
- NV
- NY
- OH
- OK
- OR
- PA
- SC
- SD
- TN
- TX
- UT
- VA
- VT
- WA
- WI.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0898-2022
- Event ID
- 89615
- Status
- Terminated
- Classification
- Class II
- Company
- FDMR, INC DBA SUJI'S KOREAN CUISINE
- Product description
- Taiyaki Variety Pack; 21.6 oz. (600g) 30 fish waffles in a units, 27 master cased to a pallet, 40 pallets to container. Item Number 1598329, UPC: 8 50013 07258 3 Three flavors: Chocolate Cream, Vanilla Custard and Red Bean & Cinnamon. Manufactured for Suji's Korean Cuisine, Seattle, WA Country of Origin: Republic of Korea.
- Quantity
- 63,451sold
- Reason
- Hazelnuts were declared in ingredient statement but not in Contains statement.
- Recall initiation date
- February 17, 2022
- Report date
- March 23, 2022
- Classification date
- Not published in this source record
- Termination date
- July 6, 2022
- Distribution pattern
- Nationwide to wholesale customer locations in AK, AL,AR,AZ,CA,CO,CT,DC, DE,FL, GA, HI,IA, ID, IL, IN, KS, KY,LA,MA,MD, MI, MN, MO, MS, MT, NA, NC, ND,NE, NH, NJ, NM, NV, NY, OH,OK,OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI.
- UPC, lot, and code information
- All lots
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Letter
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: FDMR, INC DBA SUJI'S KOREAN CUISINE
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 |
|---|---|
| Alaska | 1 |
| Alabama | 1 |
| Arkansas | 1 |
| Arizona | 1 |
| California | 1 |
| Colorado | 1 |
| Connecticut | 1 |
| District of Columbia | 1 |
| Delaware | 1 |
| Florida | 1 |
| Georgia | 1 |
| Hawaii | 1 |
| Iowa | 1 |
| Idaho | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Kansas | 1 |
| Kentucky | 1 |
| Louisiana | 1 |
| Massachusetts | 1 |
| Maryland | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| Missouri | 1 |
| Mississippi | 1 |
| Montana | 1 |
| North Carolina | 1 |
| North Dakota | 1 |
| Nebraska | 1 |
| New Hampshire | 1 |
| New Jersey | 1 |
| New Mexico | 1 |
| Nevada | 1 |
| New York | 1 |
| Ohio | 1 |
| Oklahoma | 1 |
| Oregon | 1 |
| Pennsylvania | 1 |
| South Carolina | 1 |
| South Dakota | 1 |
| Tennessee | 1 |
| Texas | 1 |
| Utah | 1 |
| Virginia | 1 |
| Vermont | 1 |
| Washington | 1 |
| Wisconsin | 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?
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