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RECALL RECORD — CLASS IIRecall closedH-0213-2026/FDA enforcement
Water Pure, INC.·Dietary Supplements·Oct 24, 2025

My Bladder

What you need to know

Class II

  • What happened

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

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. Some E. coli strains produce toxins that can cause severe, sometimes bloody diarrhea.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Recall closed · classified by the FDANationwide (US)More supplements

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameWater Pure, INC.
Recalling firmWater Pure, INC.Plainview, NY, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot Number: 03042517
Distribution area
Nationwide

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

United States, Canada, Puerto Rico

Quantity affected17, 612 bottles
Recall initiationFDA report date: December 10, 2025
FDA recall numberH-0213-2026

Beyond the headline

The recall, in context

Water Pure, INC. initiated this supplements recall on October 24, 2025. The FDA enforcement report states: Product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303. The FDA report lists distribution as: Nationwide, including Guam, Puerto Rico, and the US Virgin Islands and to Canada.

The FDA enforcement report describes the reason as: Product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303

My Bladder was made or distributed by Water Pure, INC. in Plainview, NY, United States. This page reflects FDA report H-0213-2026, dated December 10, 2025.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, some E. coli strains produce toxins that can cause severe, sometimes bloody diarrhea.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

E. coli

Symptoms to watch for

Severe stomach cramps, diarrhea, vomiting and sometimes a low fever. Bloody diarrhea or signs of dehydration need prompt medical attention.

When symptoms may appear

Usually 3 to 4 days after exposure, with a range of roughly 1 to 10 days.

Higher-risk groups

Young children, older adults, pregnant people and people with weakened immune systems are at higher risk of complications.

What to do now

  1. 1Stop using or eating the affected product and keep it away from children and pets.
  2. 2Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer.
  3. 3If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

General guidance based on CDC and FDA consumer information.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the My Bladder recall?

Water Pure, INC. recalled My Bladder in an FDA Class II enforcement action reported as H-0213-2026. Product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303

What are the symptoms of E. coli exposure?

Severe stomach cramps, diarrhea, vomiting and sometimes a low fever. Bloody diarrhea or signs of dehydration need prompt medical attention.

How quickly can E. coli symptoms appear?

Usually 3 to 4 days after exposure, with a range of roughly 1 to 10 days.

Who is most at risk from E. coli?

Young children, older adults, pregnant people and people with weakened immune systems are at higher risk of complications.

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Stop using or eating the affected product and keep it away from children and pets. Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer. If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

How do I get a refund from Water Pure, INC.?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall H-0213-2026 and keep the packaging, lot code and proof of purchase if you have them.

Is the Water Pure, INC. recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record H-0213-2026. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.