RecallHawk
Class III Recall

Fiji Natural Artesian Water 500 mL (24 pack) Case UPC Code: 6 32565 00004 3 Bottle UPC Code: 6 32565 00001 2

Natural Waters of Viti Limited

Summary

The FDA issued a Class III for Fiji Natural Artesian Water 500 mL (24 pack) Case UPC Code: 6 32565 00004 3 Bott by Natural Waters of Viti Limited. Reason: Firm testing revealed Manganese in addition to three bacterial genera..

Details

Source

Food Recall

External ID

F-1264-2024

Action Date

2024-05-29

Status

Terminated

Category

food

Product Description

Fiji Natural Artesian Water 500 mL (24 pack) Case UPC Code: 6 32565 00004 3 Bottle UPC Code: 6 32565 00001 2

Lot/Code Info: Nov. 11, 2023, Nov. 12, 2023, Nov. 13, 2023, Nov. 24, 2023, Nov. 25, 2023

Quantity Affected: 78,533 cases

Reason for Recall

Firm testing revealed Manganese in addition to three bacterial genera.

Distribution

U.S. distribution to the following: WA and nationwide online directly to consumers

Type: Voluntary: Firm initiated

Recall Initiated: 2024-03-04

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

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 (Natural Waters of Viti Limited) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Natural Waters of Viti Limited have FDA actions?

This is the only FDA action we have on record for Natural Waters of Viti Limited in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1264-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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