Reported May 28, 2014 · Terminated
PRO ArthMax Dietary Supplement tablets, 750 mg, 120 count bottles, Distributed by Human Science Foundation, Los…
Human Science Foundation
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: HUMAN SCIENCE FOUNDATION · 13722 Harvard Pl · Gardena, CA · 90249-2527
Is this the product you have?
- PRO ArthMax Dietary Supplement tablets, 750 mg, 120 count bottles, Distributed by Human Science Foundation, Los Angeles, CA
- Lot codes and dates
Lot# 220113Exp. 01/16 Lot# 800213Exp. 03/16 Lot# U133000Exp. 04/16 Lot# U143200Exp. 08/16 Lot# YJK015311Exp. 10/16
- Amount recalled
- 24,268 bottles
Where it was sold
- Nationwide
Why it was recalled
Stop using this product now
Marketed without an Approved NDA/ANDA; FDA analysis found the product to contain Chlorzoxazone, Nefopam, Diclofenac, Ibuprofen, Naproxen, and Indomethacin
Using this product could cause serious injury, illness or death — stop using it now.
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