H-0095-2025 Class III Terminated

Recalled by Preventics, Inc. Dba Legere Pharmaceuticals — Scottsdale, AZ

FDA food recall H-0095-2025 was initiated by Preventics, Inc. Dba Legere Pharmaceuticals on Apr 30, 2025 and is designated Class III. Reason for recall: Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules. The recall status is terminated (terminated Sep 18, 2025). Affected quantity: 94,190 capsules.

Recall details

Product Type
Food
Report Date
Jul 2, 2025
Initiation Date
Apr 30, 2025
Termination Date
Sep 18, 2025
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
94,190 capsules

Product description

NutriLean, dietary supplement. 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.

Distribution pattern

Distributed Nationwide in the United States.

Code information

21745-11, 21745-12, 21745-13, 21745-14, 21745-15

Source

Dataset
openFDA food recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for H-0095-2025
openFDA file date
Nov 3, 2026
Loaded by RegDataLab
Nov 8, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

Source: openFDA record for H-0095-2025. Report a data issue: hello@regdatalab.com.