US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jul 12, 2017 (9 years ago)

Testosterone Cypionate + Progesterone, 200 mg/ 2.5 mg/mL ,10 mL amber glass vials, Rx…

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

Why it was recalled

CGMP Deviations

What was recalled

Testosterone Cypionate + Progesterone, 200 mg/ 2.5 mg/mL ,10 mL amber glass vials, Rx Only, Compounded by AXIA Pharmaceutical, Los Angeles, CA 90025

Recalling firm
Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1040-2017

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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