Rodex Forte — Class III food recall H-0096-2025
Terminated recall by Preventics, Inc. dba Legere Pharmaceuticals, reported 2025-07-02, distributed nationwide. Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
| Recall number | H-0096-2025 |
|---|---|
| Product type | Food |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Preventics, Inc. dba Legere Pharmaceuticals, Scottsdale, AZ, United States |
| Recall initiated | 2025-04-30 |
| Classified | 2025-06-25 |
| Reported by FDA | 2025-07-02 |
| Terminated | 2025-09-18 |
| Distributed | Nationwide (US) |
| Quantity | 42,280 capsules |
| Reason classes | undeclared allergen |
| Lot numbers | 21635-21, 21635-22, 21635-23, 21635-34 |
Product
Rodex Forte, dietary supplement. 90 capsule bottles. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
Reason for recall
Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/H-0096-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.