Dark Mode Light Mode

Keep Up to Date with the Most Important News

By pressing the Subscribe button, you confirm that you have read and are agreeing to our Privacy Policy and Terms of Use
Follow Us
Follow Us

Emergency Recall: E. coli Found in Widely Used Dietary Supplement

Spread the love


MyBladder, a widely used dietary supplement, has been recalled by Purity Products after routine testing revealed it may contain two strains of E. coli, according to a press release issued by the U.S. Food and Drug Administration (FDA).

Why it matters

E. coli can cause gastrointestinal problems or other infections, especially in infants, children, the elderly, and individuals with compromised immune systems.

Past outbreaks, previously linked to consumer products, have sometimes resulted in hospitalizations and even deaths. In 2024, an E. coli outbreak linked to romaine lettuce infected approximately 89 U.S. citizens across 15 states, hospitalizing more than 29 and causing one death.

What you need to know

Purity Products, a company called Dwater, recalled a single lot of MyBladder dietary supplement due to potential contamination with E. coli O7:K1 and E. coli 1303.

The subject of this recall is product lot number 03042517, which was distributed nationwide through direct shipping through Walmart and Amazon websites. This supplement is packaged in a 150CC white HDPE bottle containing 60 clear brown powder capsules.

Purity Products took action Tuesday following routine product testing that revealed the presence of two strains of E. coli that are not permitted in dietary supplements under current regulatory standards.

According to the company, the contamination has been traced to a temporary change in supplier and anyone in possession of affected products is advised to immediately stop using and discard or return them to the place of purchase and request a full refund.

Anyone who experiences unexpected side effects after using the product should contact their doctor or health care provider.

what people say

In its announcement, the FDA categorized these as health risks: “Gastrointestinal or other infections, especially in vulnerable individuals such as newborns, young children, the elderly, and people with weakened immune systems.”

purity product said: “This recall is a precautionary measure to ensure consumer safety and compliance with product safety regulations.”

What happens next?

Consumers seeking additional information or a refund are encouraged to contact Richard Conant at Purity Products by calling 516-316-9486 or emailing richard.conant@purityproducts.com.

The FDA and Purity Products encourage consumers to review relevant lot numbers on MyBladder bottles they purchase and follow recall instructions to reduce exposure to associated hazards. Any side effects associated with recalled supplements must be reported to the FDA. MedWatch Adverse Event Reporting Program.

For the latest updates and official advice on this and other recalls, please visit: FDA Recalls, Market Withdrawals and Safety Alerts Page.



Source link

Keep Up to Date with the Most Important News

By pressing the Subscribe button, you confirm that you have read and are agreeing to our Privacy Policy and Terms of Use
Add a comment Add a comment

Leave a Reply

Previous Post

HTA Monthly - October 2025

Next Post

Text as effective as live video in treating depression - UW Medicine