Buckhead Tuna
Reason The Firm was notified by NJ Department of Health of two samples collected from tuna with reported high levels of scombrotoxin.
Loki Fish Wild Keta Salmon Lox recall
Recalled by Loki Fish Company - Office · Seattle, WA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Potential to be contaminated with Listeria monocytogenes.
Pathogen: Listeria
Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.
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
Loki Fish Wild Keta Salmon Lox, packaged in a 4 oz. plastic pouch, sliced on a coated board, 24 packages to a case. UPC 92103 00111. The label is read in parts: LOKI FISH *** WILD KETA LOX *** Ingredients: Wild Keta salmon, honey, salt and spices *** PRODUCT OF USA *** KEEP REFRIGERATED BELOW 38F ***lokifish.com***SEATTLE WA***".
Quantity: 237 packages
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.
There are no best by dates on the package.
Where it was sold
Oregon Washington
FDA's distribution note: distributed in Oregon and Washington.
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
- Loki Fish Company - Office
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 23, 2021
- In FDA report of
- Sep 22, 2021
- Terminated
- Jan 13, 2022
- FDA recall number
- F-1005-2021 · event 88554
- Official record
- FDA enforcement report search
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