Buckhead Tuna
Reason The Firm was notified by NJ Department of Health of two samples collected from tuna with reported high levels of scombrotoxin.
Dh. Anchovy recall
Recalled by Seafood Avenue · El Monte, CA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product may have the potential for pathogen growth and toxin formation due to Clostridium botulinum.
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
DH. ANCHOVY 2.2 Lbs.; Item No: D0161; B/C: 59033 50161; DH. ANCHOVY 3.5 oz..; Item No: D0162; B/C: 59033 50162
Quantity: 490 units
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 Codes: TTL-D1615 and TTL-H0715; Lot Codes: TTL-L1014 and TTL-K2814
Where it was sold
California Colorado Illinois Massachusetts Maryland Michigan Minnesota Pennsylvania Texas Utah Wisconsin
FDA's distribution note: CA, PA, CO, IL, WI, MA, TX, MD, MI, MN, UT
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. 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
- Seafood Avenue
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Oct 21, 2015
- In FDA report of
- Apr 5, 2017
- Terminated
- Mar 27, 2017
- FDA recall number
- F-1743-2017 · event 72473
- Official record
- FDA enforcement report search
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