RegenErect
Recalling firm: VivaCeuticals, Inc. dba Regeneca Worldwide
Why it was 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.
The exact product
RegenErect
Check the codes
Compare these FDA-provided codes, lot numbers or dates with the product you have.
Match the product, size and code together. A similar name alone does not identify your batch.
Original FDA code information
all lots
Recall details
- Recall number
- F-1820-2017
- Event ID
- 76634
- FDA status
- Terminated
- Initiated
- Mar 9, 2017
- Reported
- Apr 12, 2017
- Classified
- Mar 31, 2017
- Terminated
- Aug 8, 2017
- Quantity
- unknown
- Location
- Irvine, CA, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Press Release
Where it was distributed
US
FDA source record · F-1820-2017
Data updated September 16, 2026. View official FDA data ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.