Buckhead Tuna
Reason The Firm was notified by NJ Department of Health of two samples collected from tuna with reported high levels of scombrotoxin.
Breaded Fish with Vera Cruz Sauce recall
Recalled by Bateman Community Living · West Sacramento, CA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Internal label verification found that the breading ingredients for the fish patty were not on the ingredient statement and that wheat not listed as an ingredient or allergen. It also did not declare the correct variety of fish
Undeclared allergens: Wheat 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
Breaded Fish with Vera Cruz Sauce; In 13.4 oz 3 compartment tray that has the fish, rice pilaf and green peas. Item number KD-0003 No labeling on individual trays, only on out box of 4 meals per case.
Quantity: 8792 cases
Food: Seafood & fish Bread & bakery
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 codes: 08617, 10417, 11717, 12917, 15317, 17217 , 18717, 20617, 22117.
Where it was sold
California
FDA's distribution note: One customer in California
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 wheat, 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
- Bateman Community Living
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 28, 2017
- In FDA report of
- Sep 20, 2017
- Terminated
- Sep 21, 2017
- FDA recall number
- F-3540-2017 · event 78039
- Official record
- FDA enforcement report search
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