RecallHawk
Class II Recall

Tidal Seafood Yellowfin Tuna Poke Best Buy 6/18/2024

WORLDWIDE SEAFOOD PRODUCTS LLC

Summary

The FDA issued a Class II for Tidal Seafood Yellowfin Tuna Poke Best Buy 6/18/2024 by WORLDWIDE SEAFOOD PRODUCTS LLC. Reason: Frozen Tuna may contain elevated levels of Histamine.

Details

Source

Food Recall

External ID

F-0076-2023

Action Date

2022-10-19

Status

Terminated

Category

food

Product Description

Tidal Seafood Yellowfin Tuna Poke Best Buy 6/18/2024

Lot/Code Info: 1443

Quantity Affected: 40 cases

Reason for Recall

Frozen Tuna may contain elevated levels of Histamine

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.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-09-16

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 40 food recalls issued in the same week, part of 204 food-related FDA actions this month.

WORLDWIDE SEAFOOD PRODUCTS LLC has 3 FDA actions in our database, including 3 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (WORLDWIDE SEAFOOD PRODUCTS LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does WORLDWIDE SEAFOOD PRODUCTS LLC have FDA actions?

WORLDWIDE SEAFOOD PRODUCTS LLC has 3 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0076-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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