FDA Food recall H-0096-2025
Rodex Forte, dietary supplement. 90 capsule bottles
- FDA Food
- Class III
- terminated
- Published 2025-07-02
On 2025-07-02 the FDA classified a Class III recall of Rodex Forte, dietary supplement. 90 capsule bottles by Preventics, citing undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
Read the official FDA Food notice
| Agency | FDA Food |
|---|---|
| Recall number | H-0096-2025 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2025-04-30 |
| Published | 2025-07-02 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Preventics |
| Distribution | US |
Product
Rodex Forte, dietary supplement. 90 capsule bottles. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
Reason
Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
Identifiers
| code_info | Batch codes: 21635-21, 21635-22, 21635-23, 21635-34 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-0096-2025%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.