Why it was recalled
Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin 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)
Lot numbers, UPCs & expiration codes
Batch codes: 21635-21, 21635-22, 21635-23, 21635-34
Where it was sold
Distributed Nationwide in the United States.
What to do if you have this product
- Compare the brand, size, and lot/UPC codes on your package with the codes above.
- If it matches, don't eat it. Return it to the store for a refund or throw it away.
- Wash surfaces and containers that touched the product.
- If you feel sick after eating it, contact your doctor. In an emergency call 911.
Recall details
- Recall number
- H-0096-2025
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- Apr 30, 2025
- FDA report date
- Jul 2, 2025
- Quantity
- 42,280 capsules
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Preventics, Inc. dba Legere Pharmaceuticals
Original FDA data
Every field from FDA enforcement report H-0096-2025, exactly as published.
Show all FDA fields
- City
- Scottsdale
- State
- AZ
- Status
- Terminated
- Country
- United States
- Event ID
- 96839
- Address
- 15344 N 83rd Way Ste 101
- Code information
- Batch codes: 21635-21, 21635-22, 21635-23, 21635-34
- Postal code
- 85260-2594
- Report date
- Jul 2, 2025
- Product type
- Food
- Recall number
- H-0096-2025
- Classification
- Class III
- Recalling firm
- Preventics, Inc. dba Legere Pharmaceuticals
- Product quantity
- 42,280 capsules
- Termination date
- Sep 18, 2025
- Reason for recall
- Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Rodex Forte, dietary supplement. 90 capsule bottles. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
- Distribution pattern
- Distributed Nationwide in the United States.
- Recall initiation date
- Apr 30, 2025
- Initial firm notification
- Center classification date
- Jun 25, 2025