RecallHawk
Class III Recall

DRIED LILY FLOWERS Net Weight 2.5 oz (70g) Ingredients: Lily flower (Hemerocallis citrina) Distributed by: U.S. TRADING

U.S. Tov, Inc. dba U.S. Trading Company

Summary

The FDA issued a Class III for DRIED LILY FLOWERS Net Weight 2.5 oz (70g) Ingredients: Lily flower (Hemerocalli by U.S. Tov, Inc. dba U.S. Trading Company. Reason: Undeclared sulfites.

Details

Source

Food Recall

External ID

F-0668-2025

Action Date

2025-04-02

Status

Terminated

Category

food

Product Description

DRIED LILY FLOWERS Net Weight 2.5 oz (70g) Ingredients: Lily flower (Hemerocallis citrina) Distributed by: U.S. TRADING COMPANY Hayward, CA 94545-1130 Product of China

Lot/Code Info: Lot: 77303211 UPC: 7 21557 51100 8 BBD: 11.21.2025

Quantity Affected: 5200 packages

Reason for Recall

Undeclared sulfites

Distribution

AK, AL, AR, CA, CO, FL, HI, IA, IL, IN, KS, KY, MD, MN, MO, MS, MT, ND, NE, NV, NY, OH, OR, SD, TN, TX, UT, VA, WA, WI

Type: Voluntary: Firm initiated

Recall Initiated: 2025-03-03

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 33 food recalls issued in the same week, part of 204 food-related FDA actions this month.

U.S. Tov, Inc. dba U.S. Trading Company has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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 (U.S. Tov, Inc. dba U.S. Trading Company) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does U.S. Tov, Inc. dba U.S. Trading Company have FDA actions?

U.S. Tov, Inc. dba U.S. Trading Company has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0668-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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