Buckhead Tuna
Reason The Firm was notified by NJ Department of Health of two samples collected from tuna with reported high levels of scombrotoxin.
Premium Sustainable Atlantic Salmon recall
Recalled by Procesadora Aguas Claras LTDA. · Calbuco, N/A, Chile
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Direct customer tested Premium Sustainable Atlantic Salmon (Farm Raised) from Chile and had a positive 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
Premium Sustainable Atlantic Salmon (Farm Raised); 22 lb. case - Master carton - corrugated cardboard box. Internal Packaging: IQF vacuum packed with tray. Origin: Chili Packed for Osamu Corporation, Carson, CA For institutional use only
Quantity: 157 cases
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.
581213, Expiration 11-06-2020
Where it was sold
Alabama Arizona California Florida Georgia Washington Wyoming
FDA's distribution note: AL, AZ, CA, FL, GA, WA WY
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
- Procesadora Aguas Claras LTDA.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Mar 4, 2019
- In FDA report of
- Apr 10, 2019
- Terminated
- Jul 12, 2019
- FDA recall number
- F-1211-2019 · event 82318
- Official record
- FDA enforcement report search
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