Salted/marinated Pollock roe packaged in white plastic trays with…
Reason Use of Red #5 in Salted Pollock Roe and undeclared Red #5, Yellow #5 and Red #40 in Salted Pollock Roe.
Young Ocean brand Seasoned Alaskan Pollock Roe recall
Recalled by Young Ocean, Inc · Kent, WA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it 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).
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
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.***.
Quantity: 1300 packs
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 4/2020
Where it was sold
Washington
FDA's distribution note: distributed in WA only.
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. 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
- Young Ocean, Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 9, 2019
- In FDA report of
- Jun 12, 2019
- Terminated
- Aug 14, 2019
- FDA recall number
- F-1482-2019 · event 82855
- Official record
- FDA enforcement report search