Food Recall Check
Class II · Moderate risk Terminated Initiated Dec 28, 2021 (5 years ago)

10 oz. individually wrapped frozen tuna steaks recall

Recalled by Relish Foods, Inc. dba Gourmet Fusion Foods · El Segundo, CA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Elevated levels of histamines found in FDA consumer samples of frozen tuna steaks.

Some of these cause harm only with repeated exposure (lead in spices, for example), others act within hours (histamine poisoning from spoiled fish). All chemical contamination recalls.

What was recalled

10 oz. individually wrapped frozen tuna steaks; 4 servings per bag Important: Thaw under refrigeration immediately before use. May contain bones. Product must be cooked prior to consumption KEEP FROZEN AT -18 CELSIUS OR BELOW THAW UNDER REFRIGERATION IMMEDIATELY BEFORE USE. REMOVE FROM PLASTIC PRIOR TO THAWING. Packed for Relish Foods, Inc. DBA Gourmet Fusion Foods Inc. 200 Center Street, El Segundo, CA Product of Indonesia - wild caught. Keep frozen at 11 degrees C or below.

Quantity: 9000 lbs total

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.

Production Date: July 2021, Best before: July 2023 R11G2821D22A D2091A

Where it was sold

California

FDA's distribution note: CA 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
Relish Foods, Inc. dba Gourmet Fusion Foods
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 28, 2021
In FDA report of
Feb 2, 2022
Terminated
Jun 28, 2022
FDA recall number
F-0619-2022 · event 89320
Official record
FDA enforcement report search

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