Public Health Trace republishes official recall, outbreak, and surveillance data from CDC, FDA, USDA, WHO, and other public sources. It is an independent information service, not a medical provider, and not a substitute for professional medical advice or your local public health department's own guidance.
Please review the following before continuing:
Policy version 2026-07-21, effective July 21, 2026.
United States
TerminatedClass III
Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Super ProTHIN Plus, dietary supplement. Seven Packets with 2 tablets & 4 Capsules and 1 packet with 14 Nutrilean capsules. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC) | Not published in this source record | 55,080 pills | 12131 |
This recall shares FDA event ID 96839 with 5 other product entries in Public Health Trace.
FDA Recall United States TerminatedTerminated: September 18, 2025Historical recordClass III
FDA Recall United States TerminatedTerminated: September 18, 2025Historical recordClass III
FDA Recall United States TerminatedTerminated: September 18, 2025Historical recordClass III
FDA Recall United States TerminatedTerminated: September 18, 2025Historical recordClass III
FDA Recall United States TerminatedTerminated: September 18, 2025Historical recordClass III
Responsible company: Preventics, Inc. dba Legere Pharmaceuticals
FDA Recall United States TerminatedTerminated: September 18, 2025Historical recordClass III
FDA Recall United States TerminatedTerminated: September 18, 2025Historical recordClass III
FDA Recall United States TerminatedTerminated: September 18, 2025Historical recordClass III
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
A situation in which use of or exposure to a product is not likely to cause adverse health consequences.
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
