CLASS III Food recall · Reported 16 Oct 2019 · FDA Enforcement Report

Nori Ajitsuke 100P SK recalled by Wismettac Asian Foods

Wismettac Asian Foods is recalling Nori Ajitsuke 100P SK. The recall was initiated on 24 Sep 2019 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesAll codes
Quantity recalled329 cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0023-2020
FDA event ID
83900
Recalling firm
Wismettac Asian Foods, Santa Fe Springs, CA
Classification
Class III
Status
Terminated
Recall initiated
24 Sep 2019
FDA classified
8 Oct 2019
Reported
16 Oct 2019
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Other Reasons
Product category
Other

Timeline

24 Sep 2019Recall initiated by company
8 Oct 2019Classified by FDA+14 days
16 Oct 2019Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Incorrect seafood species listings on product label; product contains skipjack tuna (fish) and krill (shellfish).

Product as listed by the FDA

Nori Ajitsuke 100P SK 8.81 oz. (250 g) UPC 074410528288 Item #52818

Where it was distributed

U.S. distribution to the following: HI No foreign distribution.

Questions about this recall

Why was it recalled?

Incorrect seafood species listings on product label; product contains skipjack tuna (fish) and krill (shellfish).

Which lots are affected?

All codes

Where was it sold?

U.S. distribution to the following: HI No foreign distribution.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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