FDA Food recall ·
Rodex Forte, dietary supplement recall
- Recall number
- H-0096-2025
- Date
- (initiated April 30, 2025)
- Company / brand
- Legere Pharmaceuticals
15344 N 83rd Way Ste 101, Scottsdale, AZ, United States - Category
- Food › Class III
- Classification
- Class III
- Status
- Terminated
- Units affected
- 42,280 capsules
- Hazard tags
- Undeclared allergen
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Rodex Forte, dietary supplement. 90 capsule bottles. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
Why was it recalled?
Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Batch codes: 21635-21, 21635-22, 21635-23, 21635-34
Distribution
Distributed Nationwide in the United States.
What does Class III mean?
Class III means use of or exposure to the product is not likely to cause adverse health consequences (for example, a labeling violation).
Source: FDA (food), recall H-0096-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.