On October 27, 2025, Purity Products, based in Plainview, NY, issued a voluntary recall of one lot of its dietary supplement, MyBladder, due to the potential presence of harmful E. coli strains. This precautionary measure is aimed at safeguarding public health, especially for individuals at higher risk of infection.
Key Points:
- Recall applies to MyBladder lot number 03042517.
- Possible contamination with E. coli O7:K1 and E. coli 1303.
- Distributed via Walmart, Amazon, and direct consumer delivery.
- Consumers should stop use immediately and follow recall instructions.
In this article:
- What are the recall details?
- Why is this contamination dangerous?
- What should consumers do now?
- Frequently Asked Questions
- Conclusion and actions to take
- Disclaimers for healthcare professionals
- FDA announcement and link
What are the recall details?
Purity Products announced the recall after routine testing identified contamination in MyBladder lot number 03042517. The affected product comes in a white HDPE bottle with a white cap, containing 60 capsules filled with brown powder. Distribution was made via Walmart, Amazon, and direct deliveries in the U.S.
Recall Identification
| Product Name | Lot Number | Packaging Size | Distribution Channels |
|---|---|---|---|
| MyBladder | 03042517 | 150 CC bottle with 60 capsules | Walmart, Amazon, direct delivery |
Why is this contamination dangerous?
The contaminants identified—E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303—are strains that can cause gastrointestinal infections and other illnesses. These risks are particularly concerning for neonates, young children, older adults, and individuals with compromised immune systems.
E. coli strains are prohibited in dietary supplements under current regulatory standards. Purity Products attributed this issue to a temporary change in suppliers during production.
What should consumers do now?
If you possess MyBladder with lot number 03042517, discontinue use immediately and take one of the following steps:
- Return the product to the point of purchase for a full refund.
- Dispose of the product safely to avoid potential harm.
Consumers experiencing adverse effects after using the affected product should contact their healthcare provider promptly.
For further assistance, contact Purity Products:
- Contact Name: Richard Conant
- Phone: 516-316-9486
- Email: richard.conant@purityproducts.com
- Website: purityproducts.com
Frequently Asked Questions
- What caused the contamination?
The issue arose due to a temporary supplier change that introduced contaminants during production. - Can I continue using other Purity Products supplements?
This recall applies only to MyBladder lot 03042517. Other products are unaffected. - How do I ensure my product is part of the recall?
Check the lot number on your MyBladder bottle. Only lot 03042517 is recalled. - Will Purity Products compensate affected customers?
Yes. Consumers can request a full refund by returning the product to the place of purchase.
Conclusion and actions to take
This recall underscores the importance of rigorous product testing and regulatory compliance. Consumers should follow instructions to ensure their safety. Purity Products is actively addressing this issue to prevent recurrence.
Disclaimers for healthcare professionals
This article provides informational content based on publicly available FDA records. It does not constitute legal or medical advice. Professionals should consult relevant legal frameworks for decision-making.
FDA announcement and link
For full information about the FDA announcement, see the link below.
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/purity-products-announces-recall-dietary-supplement-my-bladder-because-possible-health-risk