Buckhead Tuna
Reason The Firm was notified by NJ Department of Health of two samples collected from tuna with reported high levels of scombrotoxin.
Wild Smoked Pink Salmon recall
Recalled by Loki Fish Company · Seattle, WA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Wild Smoked Pink Salmon is recalled due to a positive test result for 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
Wild Smoked Pink Salmon, 4-7 ounce portions in clear plastic package. No UPC. Label is read in parts: "***Smoked PINK SALMON***KEEP REFRIGERATED BELOW 38F***LOKI FISH CO***SEATTLE-WA***".
Quantity: total 492.32 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.
Lot: 121215 5594 or 121215 5613
Where it was sold
Florida Georgia Ohio Oregon Washington
FDA's distribution note: distributed in OR and WA and sold via mail orders to customers in FL, GA, and OH
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
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Mar 2, 2016
- In FDA report of
- Apr 13, 2016
- Terminated
- Aug 18, 2016
- FDA recall number
- F-1012-2016 · event 73437
- Official record
- FDA enforcement report search
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