RecallHawk
Class II Recall

Radish Turnip Cake (w/o shrimp): The product comes in a 900g ( 32 ounce), clear plastic package marked with UPC # 425404

Southern Taiwan LLC

Summary

The FDA issued a Class II for Radish Turnip Cake (w/o shrimp): The product comes in a 900g ( 32 ounce), clear by Southern Taiwan LLC. Reason: Undeclared Wheat Starch and Sulfites.

Details

Source

Food Recall

External ID

F-1545-2023

Action Date

2023-09-27

Status

Terminated

Category

food

Product Description

Radish Turnip Cake (w/o shrimp): The product comes in a 900g ( 32 ounce), clear plastic package marked with UPC # 425404904110. Ingredients: White Radish, Mushrooms, Fried Dried shallot, White Rice Flour.

Lot/Code Info: Expiration date 9/6/23 & 9/11/23

Quantity Affected: 40 packages

Reason for Recall

Undeclared Wheat Starch and Sulfites

Distribution

Distributed in WA

Type: Voluntary: Firm initiated

Recall Initiated: 2023-08-30

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 52 food recalls issued in the same week, part of 204 food-related FDA actions this month.

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

How often does Southern Taiwan LLC have FDA actions?

This is the only FDA action we have on record for Southern Taiwan LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1545-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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