The Recall Desk
LowFDA (Food)·H-0096-2025·Announced 2025-07-02

Rodex Forte dietary supplement recalled for undeclared food dyes

Rodex Forte dietary supplement (90-capsule bottles) is being recalled because the gelatin capsules contain undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No. 1), which are not listed on the label.

What this means for you

Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.

Our severity reasoning: This is an FDA Class III recall, which by definition is unlikely to cause adverse health consequences. The source text does not report any illnesses, injuries, or confirmed adverse events. The undeclared dyes present a labeling and transparency issue rather than an immediate health hazard.

Plain-English summary

Preventics, Inc. dba Legere Pharmaceuticals is recalling Rodex Forte dietary supplement in 90-capsule bottles distributed nationwide. The gelatin capsules contain undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No. 1) food dyes that are not declared on the product label.

The affected product was manufactured in batches 21635-21, 21635-22, 21635-23, and 21635-34. The product is sold without a UPC code at the address: Legere Pharmaceuticals, 15344 N 83rd Way, Scottsdale, AZ 85260.

Consumers who have purchased this product should stop using it. Those with questions or concerns should contact Legere Pharmaceuticals directly.

The recalled product

Product
Rodex Forte, dietary supplement. 90 capsule bottles. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
Manufacturer
Preventics, Inc. dba Legere Pharmaceuticals
Hazard
  • undeclared-food-dye
  • allergen-mislabeling

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (4)

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

Distribution

Distributed nationwide across the United States.