US Drug Recall Register
Class II · Moderate risk Terminated Initiated May 12, 2014 (12 years ago)

Testosterone Cypionate for Injection, each mL contains Testosterone Cypionate 200 mg…

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

Why it was recalled

Lack of Assurance of Sterility: Lack of sterility assurance in compounded aseptically filled injectable products.

What was recalled

Testosterone Cypionate for Injection, each mL contains Testosterone Cypionate 200 mg, also contains: Cotton Seed Oil, Benzyl Benzoate, Benzyl Alcohol, Rx Only, 10 mL, JOHN HOLLIS Pharmacist, Inc. 110 20th Avenue N, Nashville, TN 37203, 615-327-3234

Recalling firm
John W Hollis Inc
Origin
TN, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1392-2014

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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