H-0213-2026
Water Pure, Inc.
Data retrieved 2026-10-27T22:06:49.008Z
Site-assigned category (for this product recall): Contamination
Independent website; not affiliated with or endorsed by FDA. Recall information is attributed to the linked FDA record. Categories are assigned by this website using keyword rules; they are not FDA classifications or independent legal findings and may be incomplete or incorrect. A category summarizes the stated reason for the identified product recall, not a finding about the firm generally or its other products. FDA’s original reason text appears below.
Official openFDA record · FDA recalls and safety alerts
Fields as reported by FDA
Dates are formatted YYYY-MM-DD. “Not reported” means the field was absent or empty.
- recall_number
- H-0213-2026
- event_id
- 97892
- recalling_firm
- Water Pure, Inc.
- city
- Plainview
- state
- NY
- country
- United States
- 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
- reason_for_recall
- Product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303
- classification
- Class II
- FDA-reported status (not current status)
- Terminated
FDA does not update this status after recall classification. It may not reflect whether the recall is currently ongoing, completed, or terminated. - voluntary_mandated
- Voluntary: Firm initiated
- distribution_pattern
- Nationwide, including Guam, Puerto Rico, and the US Virgin Islands and to Canada
- product_quantity
- 17,612 bottles
- code_info
- Lot Number: 03042517
- recall_initiation_date
- 2025-10-24
- report_date
- 2025-12-10
- termination_date
- 2026-04-13