FDA Food recall F-1579-2017
Pharmanex Cortitrol
- FDA Food
- Class II
- terminated
- Published 2017-03-15
On 2017-03-15 the FDA classified a Class II recall of Pharmanex Cortitrol by Nu Skin Enterprises, citing nu Skin announces a voluntary field action for Pharmanex Cortitrol due to undeclared allergen; soy.
Read the official FDA Food notice
| Agency | FDA Food |
|---|---|
| Recall number | F-1579-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-02-13 |
| Published | 2017-03-15 |
| Last updated | 2026-09-13 11:49 UTC |
| Company | Nu Skin Enterprises |
| Distribution | US |
Product
Pharmanex Cortitrol. Cortisol Management. 60 Capsules
Reason
Nu Skin announces a voluntary field action for Pharmanex Cortitrol due to undeclared allergen; soy.
Identifiers
| code_info | Batches: DL06951-08, DL14251-08, DL34351-08, DL06061-08, DL27161-08 |
|---|
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-1579-2017%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.