Recall · openFDA Food Enforcement

My Bladder: FDA Recall H-0213-2026

Agency action: Oct 24, 2025Record ID: H-0213-2026
View official source ↗

What happened

Original notice title

My Bladder, recall H-0213-2026

From the archived source record

Product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303

What the official notice says to do

Check the original notice for the instructions that apply to the named product, company, and affected lots.

Read the official notice →

Status and source details

Status recorded in the archive
Terminated
FDA recall classification
Class II
Recall initiated by
Voluntary: Firm initiated
Report date
Dec 10, 2025
Termination date in the archive
Apr 13, 2026
Source checked
Jul 16, 2026
Record revision
7c87367d81ac

This is a dated record. Its current status may have changed since the source was captured. A record applies to its stated scope; it is not a safety rating for every product from a company.

Sources, dates, and coverage →

What is affected

Product
My Bladder; Supports normal bladder tone & control; Dietary Supplement; packaged in white HDPE bottle with a white cap; bottle size is 150 CC; the net contents in 60 clear capsules containing brown powder
Company
Water Pure, Inc.
Lot / identifier
Lot Number: 03042517
Market / distribution
Nationwide, including Guam, Puerto Rico, and the US Virgin Islands and to Canada