Buckhead Tuna
Reason The Firm was notified by NJ Department of Health of two samples collected from tuna with reported high levels of scombrotoxin.
Salmon fillets packaged inside Styrofoam boxes fully surrounded and covered in ice recall
Recalled by K & T Oriental Imports Inc. · Dallas, TX, 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
Salmon fillets packaged inside Styrofoam boxes fully surrounded and covered in ice, which were stored inside a temperature controlled cooler
Quantity: 3,094 kgs (161 packs)
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 number 7227-7228 with a production date of 11-8-2018
Where it was sold
New Mexico Texas
FDA's distribution note: Texas and New Mexico
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
- K & T Oriental Imports Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Nov 30, 2018
- In FDA report of
- Dec 19, 2018
- Terminated
- Feb 8, 2019
- FDA recall number
- F-0735-2019 · event 81681
- Official record
- FDA enforcement report search
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