Drug recall
RegeneArouse
FDA recall event 76634 · Class II · VivaCeuticals, Inc. dba Regeneca Worldwide
Key facts
| Event ID | 76634 |
|---|---|
| Recall numbers | F-1819-2017, F-1820-2017, F-1821-2017, F-1822-2017, F-1823-2017, F-1824-2017, F-1825-2017 |
| Recalling firm | VivaCeuticals, Inc. dba Regeneca Worldwide |
| Product type | Food |
| Products | RegeneArouse, RegeneBlast, RegeneBlend, RegeneBoost, RegeneFit and 2 more |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| 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. |
| Initiation date | Mar 9, 2017 |
| Report date | Apr 12, 2017 |
| Termination date | Aug 8, 2017 |
| City | Irvine |
| State | CA |
| Country | United States |
| FEI number | 3008857908 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: