43%

Fewer recalls than
Supplements & Specialty peers

GnuPharma — FDA Recall History & Enforcement Records

Established Player · Supplements & Specialty

Data Notice: Recall frequency varies by category and firm size; data is comparative and may not indicate actual brand safety or quality. See Methodology.

As of July 16, 2026, GnuPharma has 6 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 8 May 2017. GnuPharma is categorized under Supplements & Specialty based on their predominant recall history.

6
Total FDA recalls
9.2
Years in FDA database
0.7
Recalls per year
3,356 days(9.2 yrs)
Since last recall
0.0%
Class I (life-threatening)
0.7 recalls/yr vs Supplements & Specialty avg 2.3/yrWell Below Average

Recall activity over time for GnuPharma

How serious are GnuPharma recalls?

FDA recall classifications by severity

Class I (Life-threatening)
0.0% (0 recalls)
Class II (Moderate risk)
100.0% (6 recalls)
Class III (Minor violation)
0.0% (0 recalls)

Full FDA recall history for GnuPharma

All 6 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first

Date Product Reason Class & Status
8 May 2017Official FDA Notice GnuPharma Stress 100% Herbal Supplement 60 Capsules 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli) Class IITerminated
8 May 2017Official FDA Notice GnuPharma ECS Herbal Tea Relief SAMPLE ONLY 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli) Class IITerminated
8 May 2017Official FDA Notice GnuPharma Foundation 100% Herbal Supplement 60 Capsules 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli) Class IITerminated
8 May 2017Official FDA Notice GnuPharma Fit 100% Herbal Supplement 60 Capsules 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli) Class IITerminated
8 May 2017Official FDA Notice GnuPharma Sleep 100% Herbal Supplement 60 Capsules 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli) Class IITerminated
8 May 2017Official FDA Notice GnuPharma Relief 100% Herbal Supplement 60 Capsules 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli) Class IITerminated

Where have GnuPharma recalls occurred?

States affected across all recorded FDA enforcement actions

See individual recall notices

Where does this recall data come from?

Verification required: FoodRecallFinder.com cannot verify the safety of individual food products in your possession. Always verify the current recall status at FDA.gov before disposing of or consuming a product.

Data sourced from the FDA Recall Enterprise System via openFDA API. This information is for educational purposes only and does not constitute health or legal advice. FoodRecallFinder.com is not affiliated with or endorsed by the U.S. Food and Drug Administration.

To determine if your specific product is affected, verify that the brand name, product description, lot number, UPC code, and date range all match the recall details exactly. When in doubt contact the recalling firm or visit FDA.gov.

© 2026 FoodRecallFinder.com | Turnkey Trading Unlimited LLC. All rights reserved. FDA recall data sourced from openFDA.gov.

How we calculate these metrics →