Testosterone Cypionate 200 mg/mL Ethyl Oleate Injection recalled over sterility concerns

Recall date

June 26, 2019

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Official notice title

First Pharma Associates LLC dba Riverpoint Pharmacy recalls Testosterone Cypionate 200 mg/mL Ethyl Oleate Injection, packaged in a) 7.2 mL. b) 9.6 mL, c) 10.8mL vial, Rx only, Fir…

Recall number

D-1471-2019

FDA classification

Class II

Brand / firm

First Pharma Associates LLC dba Riverpoint Pharmacy

Sold / distributed

ID, WA only

Why it was recalled

Lack of Assurance of Sterility.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Testosterone Cypionate 200 mg/mL Ethyl Oleate Injection, packaged in a) 7.2 mL. b) 9.6 mL, c) 10.8mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252.