About 1.9 million bottles of Fiji Water have been recalled across the United States after testing found a mineral and three types of bacteria, according to a notice posted on the U.S. Food and Drug Administration’s (FDA) website last week, although the company later said that it poses “no health or safety risk.”
“We understand the frustration” and the alert “sent by Amazon does not accurately reflect the issue,” the company also said.
In response to the recall update last week, Fiji said in a statement to multiple news outlets that the FDA classification that was announced “relates to a matter from several months ago that never posed any health or safety risk.”
“It affected products that were sold through only one distributor, and 99 percent of all those affected bottles were reclaimed with the remainder in warehouses to be returned. There is no higher priority to us than the safety and quality of Fiji Water,” the statement said. “There is no health or safety risk posed from manganese or bacteria in the recalled lots of FIJI Water. Moreover, FIJI Water conducts regular testing to ensure consumers enjoy the soft, smooth taste of FIJI Water that they expect and love.”
The cases contained 24 bottles each, according to the notice, and the cases have a UPC Code of 6 32565 00004 3, while the bottle has a code of 6 32565 00001 2. The production dates are Nov. 11, 2023; Nov. 12, 2023; Nov. 13, 2023; Nov. 24, 2023; and Nov. 25, 2023.
The affected bottles of Fiji Water were sold between Feb. 1 and March 3, 2024, the firm said in its statement.
“Manganese is a cofactor for many enzymes, including manganese superoxide dismutase, arginase, and pyruvate carboxylase,” it said, adding that it is “involved in amino acid, cholesterol, glucose, and carbohydrate metabolism; reactive oxygen species scavenging; bone formation; reproduction; and immune response.
“Manganese also plays a role in blood clotting and hemostasis in conjunction with vitamin K.”