Buckhead Tuna
Reason The Firm was notified by NJ Department of Health of two samples collected from tuna with reported high levels of scombrotoxin.
Haddock Monkfish recall
Recalled by Northeast Seafood Products, Incorporated · Denver, CO, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Seafood and fin fish products potentially contaminated with Salmonella and implicated in illness outbreak
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
Haddock, Monkfish, Bone-in Trout, Grouper, Red Snapper, Red Rock Cod, Ocean Perch, Pacific Cod, Halibut, Coho Salmon, Atlantic Salmon Portions, Lane Snapper, Tilapia, All Natural Salmon Fillet, Pacific Sole, and Farm Raised Striped Bass
Quantity: 6416.49 lbs.
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/distribution dates from May 2021 to October 7, 2021.
Where it was sold
Colorado
FDA's distribution note: Restaurants and grocery stores in Colorado
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
- Northeast Seafood Products, Incorporated
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Oct 7, 2021
- In FDA report of
- Nov 10, 2021
- Terminated
- Apr 5, 2022
- FDA recall number
- F-0158-2022 · event 88839
- Official record
- FDA enforcement report search
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