← FDA ENFORCEMENT
H-0213-2026Class II

Water Pure, Inc.

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm
Water Pure, Inc.
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2025-12-10
Distribution
Nationwide, including Guam, Puerto Rico, and the US Virgin Islands and to Canada
Firm state
NY
Product quantity
17,612 bottles
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental Monitoring
Reason for recall

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

Code / lot info

Lot Number: 03042517

Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →