What happened
Original notice title
RegeneFit, recall F-1825-2017
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
- 78f6270d422b
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 →