Marketed without an Approved NDA/ANDA; FDA analysis found the product to contain Chlorzoxazone, Nefopam, Diclofenac, Ibuprofen, Naproxen, and Indomethacin
Marketed without an Approved NDA/ANDA; FDA analysis found the product to contain Chlorzoxazone, Nefopam, Diclofenac, Ibuprofen, Naproxen, and Indomethacin
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send HUMAN SCIENCE FOUNDATION to request your refund or repair — edit it as you like.
Subject: Recall D-1327-2014 — HUMAN SCIENCE FOUNDATION HUMAN SCIENCE FOUNDATION recalls PRO ArthMax Dietary Supplement tablets, 7 Hello, I own a HUMAN SCIENCE FOUNDATION recalls PRO ArthMax Dietary Supplement tablets, 750 mg, 120 count bottles, Distributed by Human Science Foundation, Los that is covered by recall D-1327-2014 from HUMAN SCIENCE FOUNDATION. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
