HUMAN SCIENCE FOUNDATION recalls PRO ArthMax Dietary Supplement tablets, 750 mg, 120 count bottles, Distributed by Human Science Foundation, Los Angeles,

Recalled May 28, 2014 · FDA recall D-1327-2014 · HUMAN SCIENCE FOUNDATION

Hazard

Marketed without an Approved NDA/ANDA; FDA analysis found the product to contain Chlorzoxazone, Nefopam, Diclofenac, Ibuprofen, Naproxen, and Indomethacin · FDA Class I

Units

24,268 bottles

Sold at

Nationwide

Description

Marketed without an Approved NDA/ANDA; FDA analysis found the product to contain Chlorzoxazone, Nefopam, Diclofenac, Ibuprofen, Naproxen, and Indomethacin

Product

PRO ArthMax Dietary Supplement tablets, 750 mg, 120 count bottles, Distributed by Human Science Foundation, Los Angeles, CA

Manufacturer(s)

HUMAN SCIENCE FOUNDATION

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →