FDAFDA · Food and drugs·Recall number D-1327-2014
PRO ArthMax Dietary Supplement tablets, 750 mg, 120 count bottles, Distributed by Human Science Foundation, Los Angeles, CA
Published May 28, 2014 · Recall initiated: January 13, 2014
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Marketed without an Approved NDA/ANDA; FDA analysis found the product to contain Chlorzoxazone, Nefopam, Diclofenac, Ibuprofen, Naproxen, and Indomethacin
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Manufacturer
- HUMAN SCIENCE FOUNDATION
- Distributor
- Nationwide
- Lot
- Lot# 220113; Exp. 01/16 Lot# 800213; Exp. 03/16 Lot# U133000; Exp. 04/16 Lot# U143200; Exp. 08/16 Lot# YJK015311; Exp. 10/16
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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