Food Recall Check
Class II · Moderate risk Terminated Initiated Dec 29, 2022 (4 years ago)

TOHATO Nagewa Snack Salty Taste recall

Recalled by Daiso California Warehouse · La Mirada, CA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Sodium caseinate declared, milk undeclared

Undeclared allergen: Milk

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

TOHATO Nagewa Snack Salty Taste 27g and 73g units UPC numbers: 4901940112036 & 4901940112005 Product sold individually, shipped 12 units per case Exported by: DAISO INDUSTRIES CO., LTD. 1-4-14 Saljo-Yoshiyukihigashi, Higashihiroshima-City, Hiroshima 739-8501 JAPAN

Quantity: 11,989 units

Food: Chips & snacks

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Best by 23.03.27 02JIBI

Where it was sold

California New Jersey Nevada New York Texas Washington

FDA's distribution note: Product was sent to Daiso stores in California, Washington, Nevada, Texas, New York and New Jersey. The firm also ships to 2 locations in Canada

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to milk; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Daiso California Warehouse
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 29, 2022
In FDA report of
Jan 18, 2023
Terminated
Jan 4, 2024
FDA recall number
F-0228-2023 · event 91425
Official record
FDA enforcement report search

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