Drug recall D-0213-2018
Product
Docetaxel Injection USP, 20 mg/mL, One-Vial Formulation, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Visakhapatnam - 530 046 INDIA, NDC 43598-611-11
Reason for recall
Defective Container: Product complaints received of defect in the seal of the Docetaxel injection vials that the aluminum seal and/or stopper is removed when the cap is flipped off.
Lots and codes
Lot #: H7044, Exp 05/19
Recall details
- Recalling firm
- Dr. Reddy's Laboratories, Inc., Princeton, NJ
- Quantity
- 1,051 vials
- Distribution
- Distributed nationwide in the USA, Uzbekistan, and Myanmar
- Type
- Voluntary: Firm initiated
- Recall initiated
- January 9, 2017
- Terminated
- December 4, 2018
Related products
- Docetaxel – drug information
- NDC 43598-611 Docetaxel · Docetaxel 20 mg/mL · Dr. Reddy's Laboratories Inc.
- NDC 43598-610 Docetaxel · Docetaxel 80 mg/4mL · Dr. Reddy's Laboratories Inc.