Buckhead Tuna
Reason The Firm was notified by NJ Department of Health of two samples collected from tuna with reported high levels of scombrotoxin.
Split Cooked King Crab Leg & Claw recall
Recalled by Odyssey Enterprises Inc · Seattle, WA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Cooked King crab legs & claws were recalled due to a contamination 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
Split Cooked King Crab Leg & Claw, repacked by Odyssey, net wt. 20 lbs. per box, keep frozen. UPC 28575 96323 The label is read in parts: "***SPLIT COOKED KING CRAB LEG & CLAW***PRODUCT OF RUSSIA***PACKED IN U.S.A. ***NET WT. 20 LBS***KEEP FROZEN***PACKED FOR: ODYSSEY BY: NORTHWEST SEAFOOD PROCESSORS INC***206 SW Michigan ST Seattle, WA 98106***FURTHER PREPARATION BEFORE SERVING AS FOLLOWS: FROM FROZEN STATE BOIL, STEAM OR BROIL FOR 8-10 MINUTES OR BAKE IN 400F OVEN FOR 8-10 MINUTES***".
Quantity: 400 cases (20 lbs. per case)
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 63043
Where it was sold
Wisconsin
FDA's distribution note: distributed in WI
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
- Odyssey Enterprises Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 1, 2016
- In FDA report of
- Sep 14, 2016
- Terminated
- Sep 8, 2016
- FDA recall number
- F-2037-2016 · event 74848
- Official record
- FDA enforcement report search
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