The outer package of the recalled product, Shirakiku Korean Seasoned Seaweed Korean Seaweed, is…
Recalling firm: Wismettac Asian Foods, Inc.
Undeclared allergens; sesame
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Dec 31, 2024.
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074410495534, 074410516031FDA code information
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Full FDA record and distribution details
Original product description
The outer package of the recalled product, Shirakiku Korean Seasoned Seaweed Korean Seaweed, is INCORRECTLY labeled as follows: (Principal Display Panel) Roasted Seaweed 10-0.91 OZ (26 G) PACKAGES (NET WT 9.1 OZ (260 G). (Back Display) ROASTED SEAWEED Organic Yaki Nori Ingredients: Organic Seaweed. Distributed by Wismettac Asian Foods, Inc. SANTA FE SPRINGS, CA 90670 PRODUCT OF KOREA UPC 074410495534 ITEM 49549B. The recalled product was distributed in cases identified as Wismettac ITEM No.51603 SEASONED SEAWEED (KOREAN IWANORI FULL 5SH X 5PKG SHIRAKIKU) NET WT 12/3.5 OZ (100 G) DISTRIBUTED BY Wismettac Asian Foods, Inc. SANTA FE SPRINGS, CA 90670 PRODUCT OF KOREA. The CORRECT outer packaging is identified as follows: (Principal Display Panel) Shirakiku KOREAN SEASONED SEAWEED KOREAN SEAWEED 5-0.7 OZ (20G) PACKAGES NET WT. 3.5 OZ (100 G) (Back Display) KOREAN SEASONED SEAWEED INGREDIENTS: CORN OIL, SEAWEED, SEASAME OIL, SALT. CONTAINS SEASAME. DISTRIBUTED BY Wismettac Asian Foods, Inc. SANTA FE SPRINGS, CA 90670 PRODUCT OF KOREA ITEM NO. 51603 UPC 074410516031
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 074410495534 | by Wismettac Asian Foods, Inc. SANTA FE SPRINGS, CA 90670 PRODUCT OF KOREA UPC 074410495534 ITEM 49549B. The recalled product was distributed in cases identified as Wismettac ITEM No.51603 SEASONED SEAWEED (KOR |
| UPC | 074410516031 | sian Foods, Inc. SANTA FE SPRINGS, CA 90670 PRODUCT OF KOREA ITEM NO. 51603 UPC 074410516031 |
Original FDA recall reason
Undeclared allergens; sesame
Recall details
- Recall number
- F-0120-2025
- Event ID
- 95518
- FDA status
- Terminated
- Initiated
- Oct 9, 2024
- Reported
- Nov 6, 2024
- Classified
- Nov 5, 2024
- Terminated
- Dec 31, 2024
- Quantity
- 432 cases (5,184 individual packages
- Location
- Santa Fe Springs, CA, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Where it was distributed
CA, AZ, TX, NM, WA, NY, and NV
Data updated September 16, 2026. View official FDA data ↗
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