TV Food LLC. Recalls Siluriformes Products Produced Without Benefit of Inspection

Recall date

February 22, 2019

Source

U.S. Department of Agriculture (USDA FSIS)

Recall number

018-2019

FDA classification

Class I

Sold / distributed

Illinois

Why it was recalled

Produced Without Benefit of Inspection

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

WASHINGTON, Feb. 22, 2019 TV Food LLC., a San Leandro, Calif. non-federally inspected establishment, is recalling approximately 27,956 pounds of Siluriformes, specifically Yellow Hito (catfish), products because the products were not presented for import re-inspection into the United States, the U.S. Department of Agricultures Food Safety and Inspection Service (FSIS) announced today. The following products are subject to recall: [ View Labels (PDF only)] 14-oz. vacuum-packed trays containing Golden Boy, FROZEN FISH CA DONG CA TRE DONG and Packed By: MAI SAO Seafood Co., LTD. printed on the label. 14-oz. vacuum-packed trays containing Golden Boy, FROZEN FISH STEAK CA TRE CAT KHUC and Packed By: MAI SAO Seafood Co., LTD. printed on the label. 12-oz. vacuum-packed trays containing Golden Boy, FROZEN FISH CA DONG CA TRE DONG LAM SACH KHONG DAU and Packed By: MAI SAO Seafood Co., LTD. printed on the label. 2 Fish/Bag Sold by weight vacuum-packed trays containing Golden Boy, FROZEN FISH CA DONG CA TRE VANG LAM SACH KHONG DAU and Packed By: MAI SAO Seafood Co., LTD. printed on the label. 3 Fish/Bag, Sold by Weight vacuum-packed trays containing Golden Boy, FROZEN FISH CA DONG CA TRE VANG and Packed By: MAI SAO Seafood Co., LTD. printed on the label. 2-lbs. vacuum-packed trays containing Golden Boy yellow catfish. These items were shipped to distributor in Chicago, Ill. and to other locations nationwide. The problem was discovered while FSIS was performing a recall effectiveness and product disposition check for FSIS recall 004-2019. There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider. FSIS is concerned that some product may be in consumers freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase. FSIS routinely conducts recall effectiveness checks to verify…