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Recalls and Warnings

Miracle Mineral Solution Danger
Beware of Products Which Promise to Treat or Cure Cancer, FDA Warns

Sexual Enhancement Supplements for Men and Women Recalled

Hyland's Baby Teething Tablets and Nighttime Teething Tablets Recalled

Woman Dies After Receiving Turmeric Infusion

Past Recalls and Warnings

If you have experienced an unexpected and adverse reaction to a dietary supplement, nutritional product, or generic drug, we would like to hear about it, as we may investigate the problem.
(Date Posted: 10/29/2016)

The husband of a woman who died hours after drinking the liquid supplement Miracle Mineral Solution in 2009 believes the supplement caused her death, according a recent ABC News article and feature segment on ABC's 20/20 in October 2016. His wife experienced diarrhea, nausea, and vomiting approximately 15 minutes after taking the supplement, and hours later lost consciousness and passed away. The cause of her death was ruled as "unascertained." 

The FDA warned consumers in 2010 not to use Miracle Mineral Solution, which contains sodium chlorite and, when used as directed, produces an industrial bleach that can cause nausea, vomiting, diarrhea, and symptoms of severe dehydration. Miracle Mineral Solution has been promoted as a "miracle cure" for a variety of diseases and conditions such as cancer, AIDS, malaria, autism, hepatitis, Lyme disease, asthma and the common cold. 

The couple bought the supplement while sailing near the Vanuatu islands, located between Australia and Fiji; however, the supplement appears to be available for sale in the U.S. through at least one website.

In 2015, the operator of a business called "Project GreenLife" was sentenced to more than four years in federal prison for selling Miracle Mineral Supplement in the U.S. 

See Related Warnings:

FDA Warns Against "Miracle" Mineral Supplement

Marketer Prohibited From Promoting Mineral "Cure" For Autism

To read the complete ABC News article, use the red link below.

For other Recalls and Warnings click HERE.
For information about reporting serious reactions and problems with medical products to the U.S. Food and Drug Administration through its MedWatch reporting program, please go to


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