Recall record at a glance
| Official record | F-0588-2020 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Ongoing |
| Recalling firm | Truong Phu Xanh Co., |
| Report date | Feb 5, 2020 |
| Recall initiation date | Sep 10, 2019 |
| Quantity | 915,510 pounds plus 3,645 cases |
| Location | Quang Ngai, N/A, Vietnam |
Official product description
Frozen Yellowfin Tuna, Product of Vietnam, Packaged under the following brands and cuts: Tidal Seafood Tuna Round Steak, size 6 - 8 oz, Size 8 - 10 oz, pack 2X10 lbs; and Sea Mart PREMIUM FROZEN YELLOWFIN TUNA LOINS 5-8 LBS IVP, 30 LBS; Sea Mart GRADE AAA FROZEN YELLOWFIN TUNA SAKU 12-16 IVP, 10 LBS; Sea Mart PREMIUM FROZEN YELLOWFIN TUNA STEAKS 8 OZ IVP, 10 LBS; Sea Mart GRADE AAA TUNA CUBE 0.8 OZ IVP, 10 LBS; and PACIFICA FROZEN SEAFOODS, Tuna Round Steak Size 6 OZ IVP, 20 LBS; Tuna Round Steak Size 8 OZ IVP, 20 LBS; J DELUCA FISH COMPANY, INC. TUNA LOIN CC 5 -8 LBS IVP, 30 LBS; TUNA CUBE SIZE 1 INCH IVP, 10 LBS; TUNA SAKU 10-12 OZ IVP, 10 LBS; TUNA SAKU 12-16 OZ IVP, 10 LBS; and Packaged under the FULL MOON FISH Brand - TUNA LOIN 1-3 LBS IVP, 30 LBS; TUNA LOIN 3 -5 LBS IVP 30 LBS; TUNA LOIN 5- 8 LBS IVP 30 LBS; TUNA STEAK 4 OZ IVP, 10 LBS; TUNA STEAK 6 OZ IVP, 10 LBS; TUNA STEAK 8 OZ IVP, 10 LBS; TUNA SAKU 8 -12 OZ IVP, 10 LBS; TUNA SAKU 12-16 OZ IVP, 10 LBS; FROZEN YELLOWFISH TUNA CUBE 2.8 CM IVP, 10 LBS; and TUNA KING brand - TUNA LOIN 5 -8 LBS IVP, 30 LBS; TUNA MEDALLIONS 2-3 OZ IVP, 10 LBS; TUNA STEAK 4 OZ IVP, 10 LBS; TUNA STEAK 6 OZ IVP, 10 LBS; TUNA STEAK 8 OZ IVP, 10 LBS; TUNA SAKU 12-16 OZ IVP, 10 LBS; and MiCal SEAFOOD Brand: Tuna Loins AAA 3-5LB IVP, 30lb; Tuna Loins AAA 5-8 LB IVP, 30 lb.; Tuna POKE AAA 1.5 cm IVP and 2cm IVP, 10 lb.; Tuna Steaks AAA, 4oz, 6oz, 8oz, 1 oz, 10 lb., IVP and Tuna Steaks AA 4oz, 6oz, 8oz, 10 oz, 10 lb.; Tuna Ground Meat AAA IVP, 10 lb.; Tuna Saku AAA 8-12 OZ IVP, 10 lb., Tuna Saku 12-16 oz IVP, 10lb. .
Why the product was recalled
Elevated histamine levels.
Distribution information
Direct Distribution to FL, RI, CA, NJ
How to read the classification
FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
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