Recall · openFDA Food Enforcement

RegeneSlim: FDA Recall F-1819-2017

Agency action: Mar 9, 2017Record ID: F-1819-2017
View official source ↗

What happened

Original notice title

RegeneSlim, recall F-1819-2017

From the archived source record

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.

What the official notice says to do

Check the original notice for the instructions that apply to the named product, company, and affected lots.

Read the official notice →

Status and source details

Status recorded in the archive
Terminated
FDA recall classification
Class II
Recall initiated by
Voluntary: Firm initiated
Report date
Apr 12, 2017
Termination date in the archive
Aug 8, 2017
Source checked
Jul 16, 2026
Record revision
4a23ec2ebeca

This is a dated record. Its current status may have changed since the source was captured. A record applies to its stated scope; it is not a safety rating for every product from a company.

Sources, dates, and coverage →

What is affected

Product
RegeneSlim
Company
VivaCeuticals, Inc. dba Regeneca Worldwide
Lot / identifier
Lot AAMXG
Market / distribution
US