Class IITerminated in FDA datasetRecall initiated Oct 24, 2025

My Bladder; Supports normal bladder tone & control; Dietary Supplement; packaged in white HDPE…

Recalling firm: Water Pure, Inc.

Why it was recalled

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

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Apr 13, 2026.

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ProductMy 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

FDA code information

Lot Number: 03042517

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Full FDA record and distribution details

Original product description

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

Extracted codes and context

TypeCode / valueContext
lot03042517Lot Number: 03042517

Original FDA recall reason

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

Recall details

Recall number
H-0213-2026
Event ID
97892
FDA status
Terminated
Initiated
Oct 24, 2025
Reported
Dec 10, 2025
Classified
Nov 28, 2025
Terminated
Apr 13, 2026
Quantity
17,612 bottles
Location
Plainview, NY, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Nationwide, including Guam, Puerto Rico, and the US Virgin Islands and to Canada

FDA source record · H-0213-2026

Data updated September 16, 2026. View official FDA data ↗

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