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

🕒︎ 2025-10-29

Copyright Newsweek

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

MyBladder, a widely used dietary supplement, has been urgently recalled by Purity Products after routine testing found that it may contain two strains of E. coli, according to a press release published by the Food and Drug Administration (FDA). Why It Matters E. coli can cause gastrointestinal issues or other infections, particularly in babies, young children, older adults, and individuals with compromised immune systems. Past outbreaks that have previously been linked to consumer goods, have sometimes resulted in hospitalizations and even deaths. In 2024, E. Coli linked to romaine lettuce infected around 89 U.S. citizens across 15 states, hospitalizing over 29 and causing one death. What To Know Purity Products, under the company name Dwater, has recalled a single lot of its MyBladder dietary supplement due to potential contamination with E. coli O7:K1 and E. coli 1303. The recall covers products under lot number 03042517, which was distributed nationwide via direct delivery, through the Walmart and Amazon websites. The supplement is packaged in 150 CC white HDPE bottles containing 60 clear capsules of brown powder. Purity Products took action on Tuesday, following routine product testing that revealed the presence of two E. coli strains, which are not permitted in dietary supplements by current regulatory standards. According to the company, the contamination was traced back to a temporary change in suppliers, and it's advised anyone who possesses the affected products to discontinue use immediately, and either discard it or return it to the place of purchase and request a full refund. Anyone who develops unexpected side effects after using the product should contact their physician or healthcare provider. What People Are Saying In its announcement, the FDA classified this as a health risk that could lead to “gastrointestinal or other infections, particularly in vulnerable individuals such as neonates, young children, older adults, and those with weakened immune systems.” Purity Products said: "This recall is a precautionary measure to ensure consumer safety and adherence to product safety regulations." What Happens Next Consumers seeking additional information or refunds have been advised to contact Richard Conant at Purity Products by calling 516-316-9486 or emailing richard.conant@purityproducts.com. The FDA and Purity Products are encouraging consumers to review any purchased bottles of MyBladder for the implicated lot number and to follow recall instructions to reduce their exposure to any associated risks. Any adverse reactions linked to the recalled supplement should be reported to the FDA's MedWatch Adverse Event Reporting program.

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