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VivaCeuticals, Inc.

FEI 3008857908 · 2 Park Plz Ste 1200, Irvine, California, 92614-2562, 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
2017-03-09
9 years ago

FDA record

  1. 2017-03-09
    RecallRecall F-1819-2017 · Class 2 · The firm is recalling all herbal and dietary supplements because they were not manufactured in compliance with the current Good Manufacturing Practice regulations for Dietary Supplements.
    RegeneSlim
    Source: FDA Enforcement Reports
  2. 2017-03-09
    RecallRecall F-1820-2017 · Class 2 · The firm is recalling all herbal and dietary supplements because they were not manufactured in compliance with the current Good Manufacturing Practice regulations for Dietary Supplements.
    RegenErect
    Source: FDA Enforcement Reports
  3. 2017-03-09
    RecallRecall F-1821-2017 · Class 2 · The firm is recalling all herbal and dietary supplements because they were not manufactured in compliance with the current Good Manufacturing Practice regulations for Dietary Supplements.
    RegeneArouse
    Source: FDA Enforcement Reports
  4. 2017-03-09
    RecallRecall F-1822-2017 · Class 2 · The firm is recalling all herbal and dietary supplements because they were not manufactured in compliance with the current Good Manufacturing Practice regulations for Dietary Supplements.
    RegeneBlend
    Source: FDA Enforcement Reports
  5. 2017-03-09
    RecallRecall F-1823-2017 · Class 2 · The firm is recalling all herbal and dietary supplements because they were not manufactured in compliance with the current Good Manufacturing Practice regulations for Dietary Supplements.
    RegeneBoost
    Source: FDA Enforcement Reports
  6. 2017-03-09
    RecallRecall F-1824-2017 · Class 2 · The firm is recalling all herbal and dietary supplements because they were not manufactured in compliance with the current Good Manufacturing Practice regulations for Dietary Supplements.
    RegeneBlast
    Source: FDA Enforcement Reports
  7. 2017-03-09
    RecallRecall F-1825-2017 · Class 2 · The firm is recalling all herbal and dietary supplements because they were not manufactured in compliance with the current Good Manufacturing Practice regulations for Dietary Supplements.
    RegeneFit
    Source: FDA Enforcement Reports
  8. 2017-02-08
    Compliance actionFDA Injunction (CFSAN)
    FDA source
  9. 2014-09-03
    InspectionFDA inspection · Classification: Official Action Indicated (OAI)
    Project area: Food Composition, Standards, Labeling and Econ
    FDA source
  10. 2014-08-04
    RecallRecall F-2403-2014 · Class 2 · RegeneSlim was found to contain DMAA by FDA analysis.
    RegeneSlim Appetite Control, 2 capsules/ packet, Dietary Supplement
    Source: FDA Enforcement Reports
  11. 2012-08-28
    Warning letterFDA Warning Letter (CFSAN)
    FDA source
  12. 2012-02-23
    InspectionFDA inspection · Classification: Official Action Indicated (OAI)
    Project area: Food Composition, Standards, Labeling and Econ
    FDA source
  13. 2011-05-02
    InspectionFDA inspection · Classification: Official Action Indicated (OAI)
    Project area: Food Composition, Standards, Labeling and Econ
    FDA source