RecallHawk
Class III Recall

WHH A&D Calcium Milk Drink 220ml Plastic bottles 6 bottles in 1 pack Made in China

Titans Global Inc.

Summary

The FDA issued a Class III for WHH A&D Calcium Milk Drink 220ml Plastic bottles 6 bottles in 1 pack Made in Chi by Titans Global Inc.. Reason: Product was found to have milk not declared on the ingredient label.

Details

Source

Food Recall

External ID

F-0649-2023

Action Date

2023-03-29

Status

Terminated

Category

food

Product Description

WHH A&D Calcium Milk Drink 220ml Plastic bottles 6 bottles in 1 pack Made in China

Lot/Code Info: none

Quantity Affected: 12,000 units

Reason for Recall

Product was found to have milk not declared on the ingredient label

Distribution

Product distributed exclusively within the state of CA, regionally near Los Angeles.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-02-21

Company

Titans Global Inc.

City Of Industry, CA

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

Titans Global Inc. has 4 FDA actions in our database, including 4 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 (Titans Global Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Titans Global Inc. have FDA actions?

Titans Global Inc. has 4 FDA actions in our database, including 4 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0649-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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