FDA recall record

Shirakiku Distributed by: Wismettac Asian Foods, Inc. 13409 Orden Drive Santa Fe Springs, CA recall — FDA F-0695-2023

Product was found to have the incorrect crustacean named on products

Class IIIclassification
F-0695-2023official record ID
Apr 12, 2023report date

Recall record at a glance

Official recordF-0695-2023
CategoryFood Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmWismettac Asian Foods, Inc.
Report dateApr 12, 2023
Recall initiation dateMar 20, 2023
Quantity21,816 individual packages
LocationSanta Fe Springs, CA, United States

Official product description

FURIKAKE SEASONED ROASTED SEAWEED FLAKES SEAFOOD Product number: 38245 Brand name: Shirakiku Distributed by: Wismettac Asian Foods, Inc. 13409 Orden Drive Santa Fe Springs, CA 90670

Why the product was recalled

Product was found to have the incorrect crustacean named on products

Distribution information

AL, AZ, CA, CO, CT, GA, HI, ID, MA, NC, NJ, NV, NY, OH, OR, PA, RI, SC, TN, TX, UT, WA

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.