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Class IITerminated in FDA datasetRecall initiated May 16, 2019

CHOCOLATE TAKENOKO NO SATO MEIJI (Chocolate wheat snack, 2.46 oz. Item number 65880

Recalling firm: Wismettac Asian Foods, INC

Why it was recalled

Some chocolate products imported from Japan do not have the English label for Nutrition facts, ingredients or allergens, which include milk, soy, egg, tree nuts.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jul 5, 2019.

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Compare the exact product and package details with the label you have.

ProductCHOCOLATE TAKENOKO NO SATO MEIJI (Chocolate wheat snack, 2.46 oz. Item number 65880 UPC 074410658809 - only on those bars with English labeling. Distributed by Wismettac Asian Foods, Inc.
Package size2.46 oz
UPC074410658809

FDA code information

Bars with Japanese Bar code of JAN(4902777111650)

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

CHOCOLATE TAKENOKO NO SATO MEIJI (Chocolate wheat snack, 2.46 oz. Item number 65880 UPC 074410658809 - only on those bars with English labeling. Distributed by Wismettac Asian Foods, Inc.

Extracted codes and context

TypeCode / valueContext
UPC074410658809KENOKO NO SATO MEIJI (Chocolate wheat snack, 2.46 oz. Item number 65880 UPC 074410658809 - only on those bars with English labeling. Distributed by Wismettac Asian Foods, Inc.

Original FDA recall reason

Some chocolate products imported from Japan do not have the English label for Nutrition facts, ingredients or allergens, which include milk, soy, egg, tree nuts.

Recall details

Recall number
F-1454-2019
Event ID
82925
FDA status
Terminated
Initiated
May 16, 2019
Reported
Jun 19, 2019
Classified
Jun 12, 2019
Terminated
Jul 5, 2019
Quantity
94 cases (10 individual items in inner carton) x 8 / master case
Location
Santa Fe Springs, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

AZ, CA, CO, NV, TX, UT and one customer in Mexico

FDA source record · F-1454-2019

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

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