US Drug Recall Register
Class II · Moderate risk Terminated Initiated Mar 22, 2019 (7 years ago)

Testosterone Cypionate Injection, USP, 200 mg/mL, For IM use only, 1 mL Vial, Single…

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

Why it was recalled

Presence of Particulate Matter.

What was recalled

Testosterone Cypionate Injection, USP, 200 mg/mL, For IM use only, 1 mL Vial, Single Dose, Rx Only, Manufactured by: Cipla Ltd., Verna Goa, India, Manufactured for: Cipla USA, Inc., 1560 Sawgrass Corporate Parkway, Suite 130, Sunrise, FL 33323, NDC 69097-537-31.

Recalling firm
InvaGen Pharmaceuticals, Inc.
NDC code
69097-537-31
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1124-2019

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.

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