Class IITerminatedVoluntary: Firm initiated
Organicare Nature's Science, LLC: food recall H-0031-2026
Organicare Nature's Science, LLC of Austin, TX recalled FemiClear Daily Bladder Strength Dietary Supplement, 28 Count, UPC 817008020684, SKU FEM50060. Reason: Microbial contamination with Escherichia coli O7:K1 and E. Coli 1303. The FDA listed it as Class II in its Enforcement Report dated Oct 15, 2025; distribution: nationwide.
Record status as published: Terminated (terminated Jan 14, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- FemiClear Daily Bladder Strength Dietary Supplement, 28 Count, UPC 817008020684, SKU FEM50060
- Product quantity
- 15,075 bottles (28 ct per bottle)
- Reason for recall
- Microbial contamination with Escherichia coli O7:K1 and E. Coli 1303.
- Codes, lots and dates on the package
- Lot 111924176
- Distribution pattern
- Retail stores in all 50 states and Puerto Rico and via e-commerce
- Recalling firm
- Organicare Nature's Science, LLC, Austin, TX
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Sep 4, 2025 |
| Classified by the FDA | Oct 9, 2025 |
| Published in the Enforcement Report | Oct 15, 2025 |
| Terminated | Jan 14, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0031-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.