Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Docetaxel Injection USP Recalled by Dr. Reddy's Laboratories, Inc. Due to Defective Container: complaint for seal and cap vial...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Dr. Reddy's Laboratories, Inc. directly.
Affected Products
Docetaxel Injection USP, 80 mg/4 mL, (20 mg/mL), One-Vial Formulation, Rx only, Mfd By: Dr. Reddy's Laboratories Limited, Visakhapatnam - 530 046, Andhra Pradesh, INDIA, NDC 43598-259-40.
Quantity: 5,755 vials
Why Was This Recalled?
Defective Container: complaint for seal and cap vial issues that could lead to a lack of sterility assurance.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Dr. Reddy's Laboratories, Inc.
Dr. Reddy's Laboratories, Inc. has 163 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report