FDA Food recall F-0170-2020
BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bottle, SKU: 100-4F
- FDA Food
- Class II
- terminated
- Published 2019-11-27
On 2019-11-27 the FDA classified a Class II recall of BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bottle, SKU: 100-4F by Basic Reset, citing products do not conform to Dietary Supplement CGMP regulations.
Read the official FDA Food notice
| Agency | FDA Food |
|---|---|
| Recall number | F-0170-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-09-23 |
| Published | 2019-11-27 |
| Last updated | 2026-09-13 11:50 UTC |
| Company | Basic Reset |
| Distribution | US |
Product
BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bottle, SKU: 100-4F
Reason
Products do not conform to Dietary Supplement CGMP regulations.
Identifiers
| code_info | 1820705, 1806004, 1733404, 1815204, 1719204, W0002670, W0000304, W000325, W0003878 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:50 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0170-2020%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.