Food Recall Check
Class I · High risk Terminated Initiated Mar 8, 2013 (14 years ago)

Kameda Brand Rice Cracker Kotsubukko recall

Recalled by Nishimoto Trading Co Ltd · Santa Fe Springs, CA, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Nishimoto Trading Co. is recalling Kameda Brand Rice Cracker Kotsubukko because it contains undeclared milk.

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

Kameda Brand Rice Cracker Kotsubukko, 12/4.37 oz, Item #63018.

Quantity: 2,072 units

Food: Chips & snacks Pasta, rice & grains

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.

UPC Code 0-74410-63018-8. Expiration Dates: 2013/03/15 2013/03/27 2013/03/28 2013/03/31 2013/04/05 2013/04/17 2013/04/19 2013/04/21 2013/04/23 2013/04/24 2013/04/28 2013/05/26 2013/05/27 2013/06/03 2013/06/13 2013/06/22 2013/06/23 2013/07/03 2013/07/17 2013/07/18 2013/07/21

Where it was sold

California Hawaii Illinois

FDA's distribution note: CA, HI, IL

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. 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
Nishimoto Trading Co Ltd
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 8, 2013
In FDA report of
Apr 3, 2013
Terminated
Aug 19, 2013
FDA recall number
F-1269-2013 · event 64636
Official record
FDA enforcement report search

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