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GnuPharma Corp.

FEI 3012676428 · 7726 N Owasso Expy, Owasso, Oklahoma, 74055-3393, United States

1 warning letter on record

Per FDA, as of 2026-10-31 · Sources: FDA Data Dashboard, Import Alerts, Enforcement Reports

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Import alerts
0
Import refusals (5 years)
0
Warning letters
1
Last FDA action
2022-06-16
4 years ago

FDA record

  1. 2017-05-08
    RecallRecall F-0296-2017 · Class 2 · 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
    GnuPharma Fit 100% Herbal Supplement 60 Capsules
    Source: FDA Enforcement Reports
  2. 2017-05-08
    RecallRecall F-0297-2017 · Class 2 · 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
    GnuPharma Relief 100% Herbal Supplement 60 Capsules
    Source: FDA Enforcement Reports
  3. 2017-05-08
    RecallRecall F-0298-2017 · Class 2 · 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
    GnuPharma Sleep 100% Herbal Supplement 60 Capsules
    Source: FDA Enforcement Reports
  4. 2017-05-08
    RecallRecall F-0299-2017 · Class 2 · 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
    GnuPharma Stress 100% Herbal Supplement 60 Capsules
    Source: FDA Enforcement Reports
  5. 2017-05-08
    RecallRecall F-0300-2017 · Class 2 · 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
    GnuPharma Foundation 100% Herbal Supplement 60 Capsules
    Source: FDA Enforcement Reports
  6. 2017-05-08
    RecallRecall F-0301-2017 · Class 2 · 1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
    GnuPharma ECS Herbal Tea Relief SAMPLE ONLY
    Source: FDA Enforcement Reports