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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 97892

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
October 24, 2025
Product types
Food
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Water Pure, Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Food Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

food · product 1 of 1

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

H-0213-2026
Recall number
H-0213-2026
Initiated
October 24, 2025
Classification
Class II
Status
Terminated
Recalling firm
Water Pure, Inc.
Quantity
17,612 bottles

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot Number: 03042517

Distribution pattern

Nationwide, including Guam, Puerto Rico, and the US Virgin Islands and to Canada