My Bladder; Supports normal bladder tone & control; Dietary Supplement; packaged in white HDPE bottle with a white cap;
Summary
The FDA issued a Class II for My Bladder; Supports normal bladder tone & control; Dietary Supplement; packaged by Water Pure, Inc.. Reason: Product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303.
Details
Source
Food Recall
External ID
H-0213-2026
Action Date
2025-12-10
Status
Terminated
Category
food
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
Lot/Code Info: Lot Number: 03042517
Quantity Affected: 17,612 bottles
Reason for Recall
Product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303
Distribution
Nationwide, including Guam, Puerto Rico, and the US Virgin Islands and to Canada
Type: Voluntary: Firm initiated
Recall Initiated: 2025-10-24
Company
Plainview, NY
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 36 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Water Pure, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Water Pure, Inc. have FDA actions?
This is the only FDA action we have on record for Water Pure, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0213-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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