FDA Notice: Organic By Nature, Inc. Issues Nationwide Recall for Pure Planet Organic Parasite Cleanse; Net Wt. 174g Glass Ja
Organic By Nature, Inc. has initiated a Class III recall affecting Pure Planet Organic Parasite Cleanse; Net Wt. 174g Glass Jar; Finished Product Item # 52700 Manufactured and Distributed by: Pure Planet, Ranch due to Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop.
A public safety recall has been officially logged by the U.S. Food and Drug Administration (FDA). Consumers in possession of the affected product in nationwide, Canada and Netherlands are advised to stop use immediately and contact the manufacturer for a free remedy or refund.
“A public safety recall has been officially logged by the U.S. Food and Drug Administration (FDA). Consumers in possession of the affected product in nationwide, Canada and Netherlands are advised to stop use immediately and contact the manufacturer for a free remedy or refund.”
Key Verified Points
- •Recalling Entity: Organic By Nature, Inc.
- •Product Description: Pure Planet Organic Parasite Cleanse; Net Wt. 174g Glass Jar; Finished Product Item # 52700 Manufactured and Distributed by: Pure Planet, Rancho Dominguez, CA
- •Recall Classification: Class III
- •Reason for Recall: Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
- •Distribution Footprint: nationwide, Canada and Netherlands
- •FDA Status: Terminated
Public Safety & Consumer Recall Overview
Organic By Nature, Inc. has initiated a Class III recall affecting Pure Planet Organic Parasite Cleanse; Net Wt. 174g Glass Jar; Finished Product Item # 52700 Manufactured and Distributed by: Pure Planet, Ranch due to Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop.
Identified Hazard & Consumer Risk
Federal safety regulators and issuing authorities at the U.S. Food and Drug Administration (FDA) have documented consumer hazards associated with this product. The advisory carries an official urgency level of EXPECTED and severity classified as SEVERE.
Verified Product Specifications & Campaign Records
Geographic Distribution & Nationwide Scope
Consumer Remedy & Action Checklist
Regulatory Provenance
This bulletin is compiled directly from public safety filings logged by the U.S. Food and Drug Administration (FDA). For additional support or to report an adverse event, consult the official record at https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts.
Event Timeline & Developments
Frequently Asked Questions
What should consumers do if they own the recalled product?
Consumers should discontinue use immediately and follow the remedy instructions published by the U.S. Food and Drug Administration (FDA), which include free replacement, repair, or full refund.
Is there any cost to the consumer for recall remedies?
No. Under United States federal consumer protection laws, remedies, repairs, and safety replacements for officially recalled goods are provided free of charge.
Who is the primary federal authority overseeing this recall?
This action is monitored by the U.S. Food and Drug Administration (FDA) and logged in official federal public safety recall registries.
Official Government & Primary Citations
- U.S. Food and Drug Administration (FDA) — https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts
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