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 Hot Smoked Vacuum Packed Salmon recall
Recalled by Mike's Quality Meats, Inc. · Eagle River, AK, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Frozen Hot Smoked Vacuum-Packed Salmon packaged in 1.5 lb packages is being recalled due to missing information on the label. Specifically, "Important: Keep Frozen Until Used. Thaw under Refrigerated immediately before use". Failure to provide instructions on the label for proper storage and handling of the product can cause Clostridium botulinum to grow and produce toxin.
Pathogen: Botulism
Clostridium botulinum toxin, a risk in improperly canned or under-processed foods.
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
Frozen Hot Smoked Vacuum Packed Salmon
Quantity: 65 - 1.5lb pieces
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.
Batch number 71013 (this represents the production date) Best by date is 12/10/13
Where it was sold
Alaska Oregon
FDA's distribution note: Two restaurants - one in Alaska and one in Oregon
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
- Mike's Quality Meats, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 17, 2013
- In FDA report of
- Sep 25, 2013
- Terminated
- Sep 16, 2013
- FDA recall number
- F-1882-2013 · event 65767
- Official record
- FDA enforcement report search
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