Purity Products: Dietary Supplement for bladder support — FDA announcement Oct 28, 2025

Reported terminated

A company announcement posted by FDA. The listing date can differ from the original announcement date. The absence of a termination marker does not prove the recall is currently ongoing.

Source date Oct 28, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
Dietary Supplement for bladder support
Reason
Potential contamination with Escherichia coli O7:K1 and 1303
Classification
Not supplied
Recalling firm
Dwater
Quantity
Not supplied
Agency-reported status
Terminated in FDA listing
Source record identifier
a4d019057c1fa675

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Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityPlainview, NY. October 27, 2025— Purity Products is announcing a recall of one lot of its dietary supplement MyBladder because it has the potential to be contaminated with Escherichia coli O7:K1 and 1303. The presence of these E. coli strains may pose a risk for gastrointestinal or other infections, particularly in vulnerable individuals such as neonates, young children, older adults, and those with weakened immune systems. The recall is being conducted as a precaution to protect all consumers and uphold product safety.; The product comes in a white HDPE bottle with a white cap. The bottle size is 150 CC. The net contents in 60 clear capsules containing brown powder. The affected lot is number 030425176.; Our routine testing has detected two strains of E. coli - O7:K1 (IAI39/ExPEC) and E. coli 1303 – in lot number 030425176 of this product. These strains are not permitted in dietary supplements under current regulatory standards. Subsequent investigation indicates the problem was caused by a temporary change in suppliers.; Immediately discontinue use of any product bearing this lot number.

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Distribution

Not supplied

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Dates in the source

Fda listing date
Oct 28, 2025
Company announcement date
Oct 28, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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