RecallRadar

FDA Drug recall D-1022-2013

Testosterone Cypionate/Testosterone Propionate 180-20 mg/mL Injection, 10 mL Vial, University Compounding Pharmacy, 855-398-1800

On 2013-09-18 the FDA classified a Class II recall of Testosterone Cypionate/Testosterone Propionate 180-20 mg/mL Injection, 10 mL Vial, University Compounding Pharmacy, 855-398-1800 by University Compounding Pharmacy, citing lack of Assurance of Sterility: University Compounding Pharmacy is voluntarily recalling certain pharmacy products due to lack of assurance of sterility concerns.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1022-2013
ClassificationClass II
Statusterminated
Initiated2013-09-06
Published2013-09-18
Last updated2026-09-13 11:51 UTC
CompanyUniversity Compounding Pharmacy
DistributionUS

Product

Testosterone Cypionate/Testosterone Propionate 180-20 mg/mL Injection, 10 mL Vial, University Compounding Pharmacy, 855-398-1800.

Reason

Lack of Assurance of Sterility: University Compounding Pharmacy is voluntarily recalling certain pharmacy products due to lack of assurance of sterility concerns.

Identifiers

code_infoLot 513593, Exp11/30/2013

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1022-2013%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.