← FDA ENFORCEMENT
H-0095-2025Class III

Preventics, Inc. dba Legere Pharmaceuticals

Recalling firm
Preventics, Inc. dba Legere Pharmaceuticals
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2025-07-02
Distribution
Distributed Nationwide in the United States.
Firm state
AZ
Product quantity
94,190 capsules
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Documentation & Change Control
Reason for recall

Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.

Product description

NutriLean, dietary supplement. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)

Code / lot info

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

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Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.