Topeka, Kansas – Nearly 1.9 million cases of bottled water are being recalled nationwide by the Food and Drug Administration due to concerns of manganese and bacterial contamination. The bottled water producer, Natural Waters of Viti Limited, announced the voluntary recall of over 78,000 cases of “Fiji Natural Artesian Water” on May 23rd. The water, distributed nationally through online retailers like Amazon.com, was initially shipped to the state of Washington.
Each of the recalled cases contains 24 bottles of water, totaling approximately 1,884,792 individual bottles. The recall includes specific production dates ranging from November 11, 2023, to November 25, 2023. The Centers for Disease Control and Prevention warns about the dangers of excess manganese exposure, which can lead to brain damage and other health issues.
The recall serves as a reminder of the importance of food and drink safety regulations and the need for vigilant monitoring of water quality. Consumers are urged to check the UPC and production dates of their bottled water to determine if they are affected by the recall. It is essential for consumers to be aware of potential health risks associated with contaminated water and stay informed about product recalls to protect themselves and their families.
The FDA’s swift response to the contamination issues demonstrates a commitment to public health and safety. By taking proactive measures to remove affected products from the market, the FDA is working to prevent further health risks and ensure the well-being of consumers. This incident highlights the importance of thorough quality control processes in food and beverage production to prevent contamination and maintain consumer trust.
Overall, the recall serves as a cautionary tale about the potential risks associated with water contamination and the need for stringent safety measures in the food and beverage industry. Consumers are encouraged to remain vigilant about product recalls and take necessary precautions to safeguard their health. As investigations continue into the reasons for the contamination, it is crucial for the FDA and other regulatory agencies to address any lapses in safety protocols and prevent similar incidents in the future.