RECALLING FIRM / COMPANY
GnuPharma Corp. Recalls
Are there any recent FDA recalls involving GnuPharma Corp.?
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.
6 FDA product recordsLatest initiation: May 8, 2017
Different batch.
Check the label.
All FDA recall records involving GnuPharma Corp.
Initiated in 2017. Latest and historical records, ordered by initiation date (newest first). FDA status appears on each record.
GnuPharma Fit 100% Herbal Supplement 60 Capsules
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
E. coliView details →GnuPharma Relief 100% Herbal Supplement 60 Capsules
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
E. coliView details →GnuPharma Sleep 100% Herbal Supplement 60 Capsules
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
E. coliView details →GnuPharma Stress 100% Herbal Supplement 60 Capsules
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
E. coliView details →GnuPharma Foundation 100% Herbal Supplement 60 Capsules
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
E. coliView details →GnuPharma ECS Herbal Tea Relief SAMPLE ONLY
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
E. coliView details →Found your product? Now check the codes.
Same product name. Different batch. Details matter.