H-0096-2025 Class III Terminated

Recalled by Preventics, Inc. Dba Legere Pharmaceuticals — Scottsdale, AZ

FDA food recall H-0096-2025 was initiated by Preventics, Inc. Dba Legere Pharmaceuticals on Apr 30, 2025 and is designated Class III. Reason for recall: Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules. The recall status is terminated (terminated Sep 18, 2025). Affected quantity: 42,280 capsules.

Recall details

Product Type
Food
Report Date
Jul 2, 2025
Initiation Date
Apr 30, 2025
Termination Date
Sep 18, 2025
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
42,280 capsules

Product description

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.

Distribution pattern

Distributed Nationwide in the United States.

Code information

Batch codes: 21635-21, 21635-22, 21635-23, 21635-34

Source

Dataset
openFDA food recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for H-0096-2025
openFDA file date
Nov 3, 2026
Loaded by RegDataLab
Nov 8, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

Source: openFDA record for H-0096-2025. Report a data issue: hello@regdatalab.com.