RecallHawk
Class I Recall

Sofit, Seedless Red Dates, 12 oz package, Plastic bags, 50 packages per case

Tai Phat Wholesalers, LLC

Summary

The FDA issued a Class I for Sofit, Seedless Red Dates, 12 oz package, Plastic bags, 50 packages per case by Tai Phat Wholesalers, LLC. Reason: Undeclared sulfites.

Details

Source

Food Recall

External ID

H-0459-2026

Action Date

2026-02-11

Status

Ongoing

Category

food

Product Description

Sofit, Seedless Red Dates, 12 oz package, Plastic bags, 50 packages per case

Lot/Code Info: Barcode: 4897056443990

Quantity Affected: 10 cases with 50  12 oz packages

Reason for Recall

Undeclared sulfites

Distribution

The product was distributed to the following states: FL, GA, IA, NC

Type: Voluntary: Firm initiated

Recall Initiated: 2025-11-04

Company

Tai Phat Wholesalers, LLC

Capitol Heights, MD

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 69 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Tai Phat Wholesalers, LLC has 5 FDA actions in our database, including 5 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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 (Tai Phat Wholesalers, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Tai Phat Wholesalers, LLC have FDA actions?

Tai Phat Wholesalers, LLC has 5 FDA actions in our database, including 5 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0459-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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