US Drug Recall Register
Class II · Moderate risk Terminated Initiated Oct 1, 2019 (7 years ago)

Testosterone Cypionate 180 mg/mL/Testosterone Propionate 20mg/mL Oil Injection Solution…

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

Why it was recalled

Lack of sterility assurance.

What was recalled

Testosterone Cypionate 180 mg/mL/Testosterone Propionate 20mg/mL Oil Injection Solution, 10 mL per vial, New Vitalis Pharmacy

Recalling firm
New Vitalis Pharmacy LLC dba New Vitalis Pharmacy
Origin
KY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0523-2020

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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