Prothin dietary supplement recall

Recalled by Preventics, Inc. dba Legere Pharmaceuticals · Scottsdale, AZ, United States

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

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

See the recall's own reason text for the specifics. All other reasons recalls.

What was recalled

Prothin, dietary supplement. Seven Packets containing 2 tablets and 4 capsules. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)

Quantity: 1696 bags

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

12131

Where it was sold

Nationwide.

FDA's distribution note: Distributed Nationwide in the United States.

Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm: Preventics, Inc. dba Legere Pharmaceuticals
Initiated by: Voluntary: Firm initiated
Recall initiated: Apr 30, 2025
In FDA report of: Jul 2, 2025
Terminated: Sep 18, 2025
FDA recall number: H-0091-2025 · event 96839
Official record: FDA enforcement report search

Also recalled with it (5 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class III · Low risk Terminated Other Apr 30, 2025