Aquabest Seafood recalls Sea Mart Frozen Yellowfin Tuna Loin and 2 more: contamination
Find the official FDA enforcement report
Recall at a glance
- Recalling company
- Aquabest Seafood
- Location
- Miami, FL
- Reported by FDA
- January 29, 2020
- Recall started
- November 26, 2019
- Risk class
- Class II
- Status (latest data we have)
- Terminated
- Type
- Voluntary: Firm initiated
- Category
- Seafood
- Reason type
- Other contamination
Is my product affected?
Compare your product’s name, size and lot or date codes with the list below. A recall usually covers only specific codes.
- Sea Mart Frozen Yellowfin Tuna Loin, CO treated, skinless, boneless, bloodline removed, center cut 5-8 lbs, 30 lb package
Quantity: 9,630 lbs
Codes: Pack date 019022 and Expiry date 021022. (Julian Dates) Aquabest Seafood lot #C6021222 - Sea Mart Frozen Yellowfin Tuna Steak, CO treated, skinless, boneless, bloodline removed, 8 oz, 10lb package
Quantity: 9,450 lbs
Codes: Pack dates 019022 and 019159 with Expiry dates 021022, 021159, respectively. (Julian Dates) Aquabest Seafood lot #C6026038 - Sea Mart Frozen Yellowfin Tuna Saku, CO treated, skinless, boneless, bloodline removed, 10-12oz, 10 lb package
Quantity: 2,700 lbs
Codes: Pack date 019022 and Expiry dates 021022 (Julian Dates) Aquabest Seafood lot #C6021223
Where it was distributed
Domestic and Foreign distribution
What to do
If you have this product, check the codes above. FDA recall notices often tell consumers to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information, and if you are unsure, do not eat it. If someone becomes ill after eating a recalled food, contact a healthcare professional. See FDA’s recalls and safety alerts for company announcements.
Frequently asked questions
What was recalled?
Aquabest Seafood recalled 3 products, including Sea Mart Frozen Yellowfin Tuna Loin, CO treated, skinless, boneless, bloodline removed, center cut 5-8 lbs, 30 lb package.
Why was it recalled?
Product recalled due to potentially elevated levels of Histamines. Product supplier, TPX, is recalling product which is related to a recent scombrotoxin poisoning outbreak in US.
What does Class II mean?
FDA’s middle class: use of the product may cause temporary or medically reversible adverse health consequences, or the chance of serious harm is remote.
Where was it sold or shipped?
Domestic and Foreign distribution
What should I do if I have this product?
Compare the product name, size and lot or date codes with the details on this page. FDA recall notices often tell you to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information. If you are unsure, do not eat it.
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Sources
Data provided by the U.S. Food and Drug Administration (FDA) through openFDA, shown as published and not validated by this site. This site is independent and is not affiliated with or endorsed by FDA. It covers FDA-regulated foods; meat, poultry and egg products are regulated by USDA. Do not rely on this site for medical decisions: for health concerns contact a healthcare professional, and always follow the official notice and the company’s instructions. Terms and disclaimer.