FDAFDA · Food and drugs·Recall number D-0692-2017
Aripiprazole Tablets, 2 mg, 30 count unit dose box, Rx only, Manufactured by Apotex Inc., Toronto, Ontario, Canada, Distributed by Major Pharmaceuticals, Livonia, MI NDC 0904-6509-04
Published May 10, 2017 · Recall initiated: December 27, 2016
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Superpotent Drug; out of specification results for assay (manufacturer)
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- The Harvard Drug Group
- Distributor
- Nationwide and PR
- Lot
- LOT: T-00601 Exp: 04-2017
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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