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
- 2017-03-09RecallRecall 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.RegeneSlimSource: FDA Enforcement Reports
- 2017-03-09RecallRecall 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.RegenErectSource: FDA Enforcement Reports
- 2017-03-09RecallRecall 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.RegeneArouseSource: FDA Enforcement Reports
- 2017-03-09RecallRecall 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.RegeneBlendSource: FDA Enforcement Reports
- 2017-03-09RecallRecall 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.RegeneBoostSource: FDA Enforcement Reports
- 2017-03-09RecallRecall 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.RegeneBlastSource: FDA Enforcement Reports
- 2017-03-09RecallRecall 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.RegeneFitSource: FDA Enforcement Reports
- 2014-08-04RecallRecall F-2403-2014 · Class 2 · RegeneSlim was found to contain DMAA by FDA analysis.RegeneSlim Appetite Control, 2 capsules/ packet, Dietary SupplementSource: FDA Enforcement Reports