Aripiprazole Tablets, 2 mg, 30-count bottle, Rx only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada, M9L 1T9; Manufactured for: Apotex Corp., Weston, Florida 33326, NDC 60505-3075-3.
Reported: February 15, 2017 Initiated: December 19, 2016 #D-0471-2017
Product Description
Aripiprazole Tablets, 2 mg, 30-count bottle, Rx only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada, M9L 1T9; Manufactured for: Apotex Corp., Weston, Florida 33326, NDC 60505-3075-3.
Reason for Recall
Superpotent Drug: Product may not meet specifications throughout shelf life.
Details
- Recalling Firm
- Apotex Inc.
- Units Affected
- 67,946 bottles
- Distribution
- Nationwide in the USA
- Location
- Toronto, N/A
Frequently Asked Questions
What product was recalled? ▼
Aripiprazole Tablets, 2 mg, 30-count bottle, Rx only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada, M9L 1T9; Manufactured for: Apotex Corp., Weston, Florida 33326, NDC 60505-3075-3.. Recalled by Apotex Inc.. Units affected: 67,946 bottles.
Why was this product recalled? ▼
Superpotent Drug: Product may not meet specifications throughout shelf life.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on February 15, 2017. Severity: Low. Recall number: D-0471-2017.
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