US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Apr 10, 2025 (17 months ago)

Testosterone Cypionate Injection, USP, CIII, 200mg per mL, Rx only, 1mL Single-Dose Vial…

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

Why it was recalled

cGMP: complaints of crystals not redissolving into solution after warming and shaking the vials.

What was recalled

Testosterone Cypionate Injection, USP, CIII, 200mg per mL, Rx only, 1mL Single-Dose Vial, Distributed by Eugia US LLC, E. Windsor, NJ, Manufactured by: Eugia Specialties Limited, Telangana State, India, NDC 55150-277-01

Recalling firm
Eugia US LLC
NDC code
55150-277-01
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0363-2025

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