Buckhead Tuna
Reason The Firm was notified by NJ Department of Health of two samples collected from tuna with reported high levels of scombrotoxin.
Frozen Raw Yellowfin Tuna Ground Meat recall
Recalled by Sushi House INC. · Palisades Park, NJ, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Sushi House Inc. is conducting a voluntary recall of Heartlight Ground Tuna because it may contain histamines which exceed 50 ppm.
Undeclared allergen: Fish
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
Frozen Raw Yellowfin Tuna Ground Meat (Thunnus albacares), Grade: AAA, Net Weight: 10 lbs (100%), Wild Caught, Product of Indonesia, Imported and distributed by Heartlight Seafood LLC, 429 SW 195th Ave., Pembroke Pines, FL 33029, Production Date: 06/10/2014, Best used by 06/10/2016, UPC 207935110006
Quantity: 280 boxes
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 #128578
Where it was sold
Connecticut New Jersey New York
FDA's distribution note: CT, NJ and NY
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. The risk from an undeclared allergen is to people allergic to fish; for anyone else the product is generally not a safety concern. 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
- Sushi House INC.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Nov 5, 2014
- In FDA report of
- Dec 3, 2014
- Terminated
- Mar 18, 2015
- FDA recall number
- F-0574-2015 · event 69761
- Official record
- FDA enforcement report search
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