FemiClear Daily Bladder Strength Dietary Supplement, 28 Count, UPC 817008020684, SKU FEM50060
Summary
The FDA issued a Class II for FemiClear Daily Bladder Strength Dietary Supplement, 28 Count, UPC 817008020684, by Organicare Nature's Science, LLC. Reason: Microbial contamination with Escherichia coli O7:K1 and E. Coli 1303..
Details
Source
Food Recall
External ID
H-0031-2026
Action Date
2025-10-15
Status
Terminated
Category
food
Product Description
FemiClear Daily Bladder Strength Dietary Supplement, 28 Count, UPC 817008020684, SKU FEM50060
Lot/Code Info: Lot 111924176
Quantity Affected: 15,075 bottles (28 ct per bottle)
Reason for Recall
Microbial contamination with Escherichia coli O7:K1 and E. Coli 1303.
Distribution
Retail stores in all 50 states and Puerto Rico and via e-commerce
Type: Voluntary: Firm initiated
Recall Initiated: 2025-09-04
Company
Austin, TX
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 55 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 (Organicare Nature's Science, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Organicare Nature's Science, LLC have FDA actions?
This is the only FDA action we have on record for Organicare Nature's Science, LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0031-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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