FDA recall record

Young Ocean frozen, wrapped in plastic liner and packed in styrofoam box recall — FDA F-1482-2019

Young Ocean brand Seasoned Alaskan Pollock Roe is recalled because the label declares Hondashi ingredient but does not declare sub-ingredient bonito and…

Class IIclassification
F-1482-2019official record ID
Jun 12, 2019report date

Recall record at a glance

Official recordF-1482-2019
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmYoung Ocean, Inc.
Report dateJun 12, 2019
Recall initiation dateMay 9, 2019
Quantity1300 packs
LocationKent, WA, United States

Official product description

Young Ocean brand Seasoned Alaskan Pollock Roe, frozen, wrapped in plastic liner and packed in styrofoam box, and finally packed in cardboard box. Net wt. per pack: 1 lb. Each cardboard box contains 20/1 lb. packs. The label is read in parts: "***Seasoned Alaskan Pollock Roe ***Ingredients: Pollock Roe, Salt, Monosodium Glutamate, Ascorbic Acid, Sake, Sorbitol, Mirin, Hondashi, NaNo2, FD&C Red #40 and Yellow #5, Sodium DL-Malate *** Keep Frozen *** 1 LB***Young Ocean Inc. ***Kent, WA ***Product of U.S.A.***.

Why the product was recalled

Young Ocean brand Seasoned Alaskan Pollock Roe is recalled because the label declares Hondashi ingredient but does not declare sub-ingredient bonito and lactose (milk).

Distribution information

distributed in WA only.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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.

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