Food Recall Check
Class I · High risk Terminated Initiated Feb 19, 2021 (6 years ago)

Java Frozen Tuna Steaks recall

Recalled by Seafood Imports Distributors Inc. · San Diego, CA, United States

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

Why it was recalled

FDA Sample found Salmonella in one lot of 10 oz. frozen tuna steaks.

Pathogen: Salmonella

Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

Java Frozen Tuna Steaks - 10 oz. Net Wt. 10 lb. - Approximately 15-18 pieces individually vacuum packed. Product of Indonesia - Wild Caught.

Quantity: 245 x 10 lb. cases

Food: Seafood & fish

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.

Preferred Freezer Lot B7018983; MFG Code: AA 210070 2-1227; MFG Date 10 JUL 2020, Best By Date 10 JUL 2022, Trace Code 17055

Where it was sold

California Florida Illinois Maryland New York

FDA's distribution note: NY, IL, CA, FL, MD

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. 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
Seafood Imports Distributors Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 19, 2021
In FDA report of
Mar 24, 2021
Terminated
Apr 9, 2021
FDA recall number
F-0339-2021 · event 87378
Official record
FDA enforcement report search

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