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Natural Waters of Viti Limited Recall: Firm testing revealed Manganese in addition to three bacterial genera.

United States

TerminatedClass III

Company
Natural Waters of Viti Limited
Product
Fiji Natural Artesian Water 500 mL (24 pack) Case UPC Code:…
Recall date
March 4, 2024
Terminated
November 27, 2024
Source
FDA

Reason for recall

Firm testing revealed Manganese in addition to three bacterial genera.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Fiji Natural Artesian Water 500 mL (24 pack) Case UPC Code: 6 32565 00004 3 Bottle UPC Code: 6 32565 00001 2 Not published in this source record 78,533 cases Nov. 11, 2023, Nov. 12, 2023, Nov. 13, 2023, Nov. 24, 2023, Nov. 25, 2023

Distribution

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

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1264-2024
Event ID
94172
Status
Terminated
Classification
Class III
Company
Natural Waters of Viti Limited
Product description
Fiji Natural Artesian Water 500 mL (24 pack) Case UPC Code: 6 32565 00004 3 Bottle UPC Code: 6 32565 00001 2
Quantity
78,533 cases
Reason
Firm testing revealed Manganese in addition to three bacterial genera.
Recall initiation date
March 4, 2024
Report date
May 29, 2024
Classification date
Not published in this source record
Termination date
November 27, 2024
Distribution pattern
U.S. distribution to the following: WA and nationwide online directly to consumers
UPC, lot, and code information
Nov. 11, 2023, Nov. 12, 2023, Nov. 13, 2023, Nov. 24, 2023, Nov. 25, 2023
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Telephone
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Natural Waters of Viti Limited

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Washington 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class III mean?

A situation in which use of or exposure to a product is not likely to cause adverse health consequences.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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