---
title: "Purity Products: Dietary Supplement for bladder support — FDA announcement Oct 28, 2025 | Is It on Recall"
description: "Potential contamination with Escherichia coli O7:K1 and 1303"
url: https://isitonrecall.com/recall/fdapress-a4d019057c1fa675-purity-products-dietary-supplement-for-bladder-support/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA company announcement

# 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](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## 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

[Open the official record](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/purity-products-announces-recall-dietary-supplement-my-bladder-because-possible-health-risk)

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Plainview, 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. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Not supplied

No US distribution state could be established from this record. Check the official notice.

## 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.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/purity-products-announces-recall-dietary-supplement-my-bladder-because-possible-health-risk)

## Related records

[Supplements records](https://isitonrecall.com/product/supplements/) [Supplements records](https://isitonrecall.com/category/supplements/) [Dwater records](https://isitonrecall.com/brand/dwater/)