D-232-2013 Class II Terminated
FDA drug recall D-232-2013 was initiated by Palmer Natural Products on March 11, 2013 and is designated Class II. Reason for recall: Marketed Without an Approved NDA/ANDA: The products are unapproved drugs The recall status is terminated (terminated August 7, 2013). Affected quantity: 250 bottles.
Recall Details
- Product Type
- Drugs
- Report Date
- April 10, 2013
- Initiation Date
- March 11, 2013
- Termination Date
- August 7, 2013
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 250 bottles
Product Description
Aniracetam and Choline, Aniracetam 460 mg, Choline 76 mg, 180 capsules per bottler, non-Rx, distributed by BoostYourGrade, BoostYourGrade, LLC Orlando, FL
Reason for Recall
Marketed Without an Approved NDA/ANDA: The products are unapproved drugs
Distribution Pattern
Florida, Idaho, California and Hong Kong. This product can be ordered on line.
Code Information
All lot codes.