H-0096-2025
Preventics, Inc. dba Legere Pharmaceuticals
Data retrieved 2026-10-27T22:06:49.008Z
Site-assigned category (for this product recall): Allergen & mislabeling
Independent website; not affiliated with or endorsed by FDA. Recall information is attributed to the linked FDA record. Categories are assigned by this website using keyword rules; they are not FDA classifications or independent legal findings and may be incomplete or incorrect. A category summarizes the stated reason for the identified product recall, not a finding about the firm generally or its other products. FDA’s original reason text appears below.
Official openFDA record · FDA recalls and safety alerts
Fields as reported by FDA
Dates are formatted YYYY-MM-DD. “Not reported” means the field was absent or empty.
- recall_number
- H-0096-2025
- event_id
- 96839
- recalling_firm
- Preventics, Inc. dba Legere Pharmaceuticals
- city
- Scottsdale
- state
- AZ
- country
- United States
- 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.
- classification
- Class III
- FDA-reported status (not current status)
- Terminated
FDA does not update this status after recall classification. It may not reflect whether the recall is currently ongoing, completed, or terminated. - voluntary_mandated
- Voluntary: Firm initiated
- distribution_pattern
- Distributed Nationwide in the United States.
- product_quantity
- 42,280 capsules
- code_info
- Batch codes: 21635-21, 21635-22, 21635-23, 21635-34
- recall_initiation_date
- 2025-04-30
- report_date
- 2025-07-02
- termination_date
- 2025-09-18