Palmer Natural Products Aniracetam and Choline, Aniracetam 460 mg, Choline 76 mg, 180 recall — FDA D-232-2013
Marketed Without an Approved NDA/ANDA: The products are unapproved drugs
Overview of recall records associated with Palmer Natural Products, including dates, categories and classifications where available.
Classification mix: Class II: 7.
Marketed Without an Approved NDA/ANDA: The products are unapproved drugs
Marketed Without an Approved NDA/ANDA: The products are unapproved drugs
Marketed Without an Approved NDA/ANDA: The products are unapproved drugs
Marketed Without an Approved NDA/ANDA: The products are unapproved drugs
Marketed Without an Approved NDA/ANDA: The products are unapproved drugs
Marketed Without an Approved NDA/ANDA: The products are unapproved drugs
Marketed Without an Approved NDA/ANDA: The products are unapproved drugs
This page summarizes recall records in which the official source identifies Palmer Natural Products as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.