Recalls / Class II
Class IIH-0213-2026
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
- Type
- Food
- Affected lot / code info
- Lot Number: 03042517
- Quantity
- 17,612 bottles
Why it was recalled
Product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303
Recalling firm
- Firm
- Water Pure, Inc.
- Notification channel
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Type
- Voluntary: Firm initiated
- Address
- 200 Terminal Dr, Plainview, New York 11803-2312
Distribution
- Distribution pattern
- Nationwide, including Guam, Puerto Rico, and the US Virgin Islands and to Canada
Timeline
- Recall initiated
- 2025-10-24
- FDA classified
- 2025-11-28
- Posted by FDA
- 2025-12-10
- Status
- Completed
Source: openFDA Food Enforcement endpoint. Recall record H-0213-2026. The FDA issues recall classifications as health-hazard assessments, not legal findings.