US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 10, 2022 (4 years ago)

Testosterone Cypionate Injection, USP, 200 mg/mL, 1 mL Single-dose vial per carton, Rx…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Lack of Assurance of Sterility: Manufacturing deviation which was reported due to a microbial excursion

What was recalled

Testosterone Cypionate Injection, USP, 200 mg/mL, 1 mL Single-dose vial per carton, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512; Manufactured by: Sun Pharmaceutical Industries Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, 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-1154-2022

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