Food recall: Tidal Seafood Yellowfin Tuna Round Steaks 7 oz MED and LG Best Buy 6/17/2024 & 6/20/2024
Class II FDA enforcement event 90919. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
Frozen Tuna may contain elevated levels of Histamine
Class II, in the words of FDA
a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
WORLDWIDE SEAFOOD PRODUCTS LLC started this food recall on 16 Sep 2022. The firm address in the FDA record is in Perth Amboy, NJ. FDA put the recall in Class II. FDA event 90919 has 3 product records. The first FDA enforcement report date is 19 Oct 2022. The record gives the status Terminated, with the termination date 15 Jun 2023.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
Product shipped to a third party storage facility in Los Angeles, CA. Product was then further distributed to distributors in CA, TX, and NM.
Recalling firm
WORLDWIDE SEAFOOD PRODUCTS LLC, Perth Amboy, NJ.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
3 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-0074-2023 | Tidal Seafood Yellowfin Tuna Round Steaks 7 oz MED and LG Best Buy 6/17/2024 & 6/20/2024 | 400 cases | Class II | Terminated | 19 Oct 2022 |
| F-0075-2023 | Tidal Seafood Yellowfin Tuna Saku Block 10-15 oz Best Buy 6/17/2024 | 424 cases cases | Class II | Terminated | 19 Oct 2022 |
| F-0076-2023 | Tidal Seafood Yellowfin Tuna Poke Best Buy 6/18/2024 | 40 cases | Class II | Terminated | 19 Oct 2022 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class II: The middle of the three FDA recall classes.
The event in context
- Food events that started in 2022
- 452
- Share of these events in Class II
- 55%
- Product records in this event
- 3Median of the firm: 3
- Events of the firm on the register
- 2
Other events of the firm
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 20 Nov 2019 | 103200 - TIDAL SEAFOOD YELLOWFIN TUNA 10 lb, 2x10 lb cases and 103205 - TIDAL SEAFOOD YELLOWFIN TUNA 10 lb, 2x10 lb pack Event 84731 | Food | Class II | 1 |
Official channels
- FDA enforcement report F-0074-2023The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA: report a problemThe FDA page that shows where a report about a product goes.
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Cite this page
Recall Register. FDA enforcement event 90919. https://recallregister.com/fda/ii/90919/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA food enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
Product shipped to a third party storage facility in Los Angeles, CA. Product was then further distributed to distributors in CA, TX, and NM.
- What quantity of product is in FDA event 90919?
- The event has 3 product records. The first record gives this quantity:
400 cases
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many food recalls of 2022 have the same class?
- 55% of the 452 food events that started in 2022 are in Class II.