Marketed Without an Approved NDA/ANDA: The product is an unapproved new drug.
Marketed Without an Approved NDA/ANDA: The product is an unapproved new drug.
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 A B Nutrition, Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-196-2013 — A B Nutrition, Inc. A B Nutrition, Inc. recalls ANIRACETAM FAST ACTING NOOTROPIC Dietary Supplement Hello, I own a A B Nutrition, Inc. recalls ANIRACETAM FAST ACTING NOOTROPIC Dietary Supplement PHARMACEUTICAL GRADE 750mg 60 Capsules per bottle CTD Labs Houston, that is covered by recall D-196-2013 from A B Nutrition, Inc.. 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.
