Class IIITerminated in FDA datasetRecall initiated Apr 30, 2025

Rodex Forte, dietary supplement. 90 capsule bottles. Legere Pharmaceuticals 15344 N 83rd way,…

Recalling firm: Preventics, Inc. dba Legere Pharmaceuticals

Why it was recalled

Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Sep 18, 2025.

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ProductRodex Forte, dietary supplement. 90 capsule bottles. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)

FDA code information

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

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Full FDA record and distribution details

Original product description

Rodex Forte, dietary supplement. 90 capsule bottles. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)

Original FDA recall reason

Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.

Recall details

Recall number
H-0096-2025
Event ID
96839
FDA status
Terminated
Initiated
Apr 30, 2025
Reported
Jul 2, 2025
Classified
Jun 25, 2025
Terminated
Sep 18, 2025
Quantity
42,280 capsules
Location
Scottsdale, AZ, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

Distributed Nationwide in the United States.

FDA source record · H-0096-2025

Data updated September 16, 2026. View official FDA data ↗

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