Marketed Without an Approved NDA/ANDA: The products are unapproved drugs
Marketed Without an Approved NDA/ANDA: The products are unapproved drugs
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 Palmer Natural Products to request your refund or repair — edit it as you like.
Subject: Recall D-231-2013 — Palmer Natural Products Palmer Natural Products recalls NOOTROPA COGNITIVE ENHANCEMENT SUPPLEMENT, 4 Hello, I own a Palmer Natural Products recalls NOOTROPA COGNITIVE ENHANCEMENT SUPPLEMENT, 400 mg Aniracetam Capsules 60 count bottle, OTC Manufactured & Packaged in that is covered by recall D-231-2013 from Palmer Natural Products. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
