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FDA recall record

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 capsu...

Recall H-0213-2026Class IITerminatedOctober 24, 2025

FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.

FDA listed a termination date of April 13, 2026. openFDA does not treat this as a live recall-status tracker.

Product described in an FDA recall

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

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

Products involved

Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.

  • 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 information listed by FDA

Lot Number: 03042517

Distribution and firm information

Recalling firm listed by FDA: Water Pure, Inc.

Firm location listed by FDA: Plainview, NY, United States

Distribution reported by FDA: Nationwide, including Guam, Puerto Rico, and the US Virgin Islands and to Canada

Product quantity listed by FDA: 17,612 bottles

Source

Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.

Official FDA openFDA food enforcement record

Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.