Dr. Reddy's Laboratories, Inc. recalls Bortezomib, 3.5 mg/vial, Single-Dose Vial, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Visakhapatnam - 530 046,
Recalled March 2, 2022 · FDA recall D-0577-2022 · Dr. Reddy's Laboratories
Hazard
Failed stability specifications · FDA Class III
Units
2,980 vials
Sold at
USA Nationwide
Description
Failed stability specifications
Product
Bortezomib, 3.5 mg/vial, Single-Dose Vial, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Visakhapatnam - 530 046, India, NDC 43598-865-60
Manufacturer(s)
Dr. Reddy's Laboratories, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →