CLASS II Food recall · Reported 12 Apr 2017 · FDA Enforcement Report
RegeneFit recalled by VivaCeuticals
VivaCeuticals is recalling RegeneFit. The recall was initiated on 9 Mar 2017 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-1825-2017
- FDA event ID
- 76634
- Recalling firm
- VivaCeuticals, Irvine, CA
- Brand
- RegeneFit
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 9 Mar 2017
- FDA classified
- 31 Mar 2017
- Reported
- 12 Apr 2017
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Manufacturing (CGMP) Deviations
- Product category
- Other
Timeline
| 9 Mar 2017 | Recall initiated by company | |
| 31 Mar 2017 | Classified by FDA | +22 days |
| 12 Apr 2017 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
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.
Product as listed by the FDA
RegeneFit
Where it was distributed
US
Questions about this recall
Is RegeneFit recalled?
Yes. VivaCeuticals recalled RegeneFit on 9 Mar 2017. The recall is Class II and its status is Terminated. Recall number F-1825-2017.
Why was it recalled?
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.
Which lots are affected?
LOT B1109329
Where was it sold?
US
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from VivaCeuticals
All 7| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS II | RegenErect recalled by VivaCeuticalsRegenErect | VivaCeuticals | Manufacturing (CGMP) Deviations | CA |
| Food | CLASS II | RegeneBoost recalled by VivaCeuticalsRegeneBoost | VivaCeuticals | Manufacturing (CGMP) Deviations | CA |
| Food | CLASS II | RegeneBlast recalled by VivaCeuticalsRegeneBlast | VivaCeuticals | Manufacturing (CGMP) Deviations | CA |
| Food | CLASS II | RegeneArouse recalled by VivaCeuticalsRegeneArouse | VivaCeuticals | Manufacturing (CGMP) Deviations | CA |
| Food | CLASS II | RegeneBlend recalled by VivaCeuticalsRegeneBlend | VivaCeuticals | Manufacturing (CGMP) Deviations | CA |
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