Buckhead Tuna
Reason The Firm was notified by NJ Department of Health of two samples collected from tuna with reported high levels of scombrotoxin.
IQF Oysters recall
Recalled by Korean Farm, INC. · Santa Fe Springs, CA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Korean Farm is recalling Assi Brand Korean Oysters because they have been prepared, packed, or held under insanitary conditions whereby they may have become contaminated with filth, or whereby they may have been rendered injurious to health.
These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.
What was recalled
IQF Oysters 3lbs, Assi Brand, Item# 20083K,10x3 lb; Oyster Block, Assi Brand, item# 20085K, 30x1 lb; Oysters 8 oz - Tiny, Assi Brand, item# 20086, 40x8 oz; IQF Oysters 20 oz - Tiny, Assi Brand, item#20093, 20x20 oz.
Quantity: 638 cartons
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.
IQF Oysters 3lbs: UPC # 10081652200830, LOT # DO10921. Oyster Block: UPC # 10081652200854, LOT # DO10921. IQF Oysters 8 oz: UPC # 10081652200861, LOT # C-110304, DO11071. IQF Oysters 20 oz: UPC # 10081652200939, LOT # DO11021.
Where it was sold
Nationwide.
FDA's distribution note: Nationwide in the US.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. 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
- Korean Farm, INC.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jun 14, 2012
- In FDA report of
- Jul 18, 2012
- Terminated
- Mar 8, 2013
- FDA recall number
- F-1742-2012 · event 51667
- Official record
- FDA enforcement report search
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