US Drug Recall Register
Class III · Low risk Terminated Initiated Jan 11, 2021 (6 years ago)

Testosterone Cypionate Injection, USP CIII 200mg/ml FOR INTRAMUSCULAR USE ONLY 1mL…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Incorrect Labeling: Incorrect lot number on secondary packaging

What was recalled

Testosterone Cypionate Injection, USP CIII 200mg/ml FOR INTRAMUSCULAR USE ONLY 1mL Single-dose vial Distributed by: Sun Pharma Ind. Inc, NJ 08512 Manufactured by: Sun Pharma Ind. Ltd., India NDC 62756-015-40

Recalling firm
Sun Pharmaceutical Industries INC
NDC code
62756-015-40
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0242-2021

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

Other Testosterone recalls

See all