PlainRecalls
FDA Drug Moderate Class II Terminated

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

Reported: December 4, 2019 Initiated: October 1, 2019 #D-0523-2020

Product Description

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

Reason for Recall

Lack of sterility assurance.

Details

Units Affected
2981.62 mL
Distribution
Distributed Nationwide in the USA
Location
Louisville, KY

Frequently Asked Questions

What product was recalled?
Testosterone Cypionate 180 mg/mL/Testosterone Propionate 20mg/mL Oil Injection Solution, 10 mL per vial, New Vitalis Pharmacy. Recalled by New Vitalis Pharmacy LLC dba New Vitalis Pharmacy. Units affected: 2981.62 mL.
Why was this product recalled?
Lack of sterility assurance.
Which agency issued this recall?
This recall was issued by the FDA Drug on December 4, 2019. Severity: Moderate. Recall number: D-0523-2020.