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Class II: temporary or reversible health riskTerminated

Water Pure My Bladder Recall

My Bladder

Water Pure, Inc. · Plainview, NY

Risk level
Class II
Reported by FDA
Dec 10, 2025
Recall ID
H-0213-2026
Check your lot numberHow we source this data

Summary

Water Pure recalled My Bladder starting Oct 24, 2025. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report H-0213-2026 on Dec 10, 2025. Reason: Product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303. Status: Terminated.

Why it was recalled

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

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

Lot numbers, UPCs & expiration codes

Lot Number: 03042517

Where it was sold

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

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
H-0213-2026
Classification
Class II
Status
Terminated
Recall initiated
Oct 24, 2025
FDA report date
Dec 10, 2025
Quantity
17,612 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Water Pure, Inc.

Original FDA data

Every field from FDA enforcement report H-0213-2026, exactly as published.

Show all FDA fields
City
Plainview
State
NY
Status
Terminated
Country
United States
Event ID
97892
Address
200 Terminal Dr
Code information
Lot Number: 03042517
Postal code
11803-2312
Report date
Dec 10, 2025
Product type
Food
Recall number
H-0213-2026
Classification
Class II
Recalling firm
Water Pure, Inc.
Product quantity
17,612 bottles
Termination date
Apr 13, 2026
Reason for recall
Product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303
Voluntary / mandated
Voluntary: Firm initiated
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
Distribution pattern
Nationwide, including Guam, Puerto Rico, and the US Virgin Islands and to Canada
Recall initiation date
Oct 24, 2025
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Nov 28, 2025

How we source this data

Source: U.S. Food and Drug Administration enforcement report H-0213-2026, published Dec 10, 2025. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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How we source and update recall data · Report incorrect information

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