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RECALLING FIRM / COMPANY

Naturex Inc. Recalls

Are there any recent FDA recalls involving Naturex Inc.?

0 recall records initiated in the snapshot’s last 365 days. 0 are FDA-listed ongoing with no termination date.FDA data updated September 16, 2026 · Snapshot assessed September 18, 2026

The FDA identifies this company as the recalling firm; this does not establish that it is the manufacturer, retailer or brand owner. “Recent ongoing” means initiated within 365 days of September 18, 2026, FDA status “Ongoing,” and no termination date. This snapshot cannot confirm what is active today.

4 FDA product recordsLatest initiation: Jun 9, 2014

Same product name.
Different batch.
Check the label.

All FDA recall records involving Naturex Inc.

Initiated in 2014. Latest and historical records, ordered by initiation date (newest first). FDA status appears on each record.

3 recall recordsPage 1 of 1
Class III
FDA status: Terminated

Echinacea Agustifolia Root PE 4:1 The product is in powder form extracted from the Echinacea root packed in varying…

Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR 180.507.

OtherView details →
Class III
FDA status: Terminated

Echinacea Agustifolia PE 4& echinosides The product is in powder form extracted from the Echinacea root packed in…

Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR 180.507.

OtherView details →
Class III
FDA status: Terminated

Echinacea Angustifolia Root PE 4: The product is in powder form extracted from the Echinacea root packed in varying…

Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR 180.507.

OtherView details →

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Same product name. Different batch. Details matter.

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