RECALLING FIRM / COMPANY
Naturex Inc. Recalls
Are there any recent recalls involving Naturex Inc.?
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
Different batch.
Check the label.
Latest recalls involving Naturex Inc.
Most recently initiated in the available FDA data; these are not necessarily active recalls.
All recall records involving Naturex Inc.
Latest and historical records, ordered by initiation date (newest first). FDA status appears on each record.
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 →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 →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 →Dried Brewers Yeast TG_YFS004 Naturex 375 Huyler Street, South Hackensack, NJ 07606 USA Phone: 1 201 440 5000 Net Wt 25…
The affected lots were tested and found to contain an unusual high level of selenium.
OtherView details →Found your product? Now check the codes.
Same product name. Different batch. Details matter.