FDA Food recall F-1825-2017
RegeneFit
- FDA Food
- Class II
- terminated
- Published 2017-04-12
On 2017-04-12 the FDA classified a Class II recall of RegeneFit by Vivaceuticals, citing 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 Supp….
Read the official FDA Food notice
| Agency | FDA Food |
|---|---|
| Recall number | F-1825-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-03-09 |
| Published | 2017-04-12 |
| Last updated | 2026-09-13 11:49 UTC |
| Company | Vivaceuticals |
| Distribution | n/a |
Product
RegeneFit
Reason
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.
Identifiers
| code_info | LOT B1109329 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:49 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1825-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.