Class ITerminated in FDA datasetOct 9, 2024

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)…

Recalling firm: Wismettac Asian Foods, Inc.

Why it was recalled

Undeclared allergens; sesame

Check the codes ↓

The exact product

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

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA code information

All Best By Dates

TypeCode / valueContext
UPC074410495534 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
UPC074410516031sian Foods, Inc. SANTA FE SPRINGS, CA 90670 PRODUCT OF KOREA ITEM NO. 51603 UPC 074410516031

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

FDA source record · F-0120-2025

Data updated September 16, 2026. View official FDA data ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.