FDA recall H-0213-2026 · Dec 10, 2025
Water Pure, Inc.: My Bladder recall
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
Reason for recall
Product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your package, and look for the company's notice on FDA's recalls page. If you have the product and aren't sure, don't use it until you've checked.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Terminated
- Codes, lots and dates
- Lot Number: 03042517
- Quantity
- 17,612 bottles
- Distribution
- Nationwide, including Guam, Puerto Rico, and the US Virgin Islands and to Canada
- Recalling firm
- Water Pure, Inc., Plainview, NY
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2025-10-24
Source: openFDA enforcement record H-0213-2026 · search recall number H-0213-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 14, 2026, 1:15 AM EDT. The agency notice is the final word.
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