Testosterone Cypionate/Testosterone Propionate 180-20 mg/mL Injection — Class II drug recall D-1022-2013
Terminated recall by University Compounding Pharmacy, reported 2013-09-18, distributed nationwide. Lack of Assurance of Sterility: University Compounding Pharmacy is voluntarily recalling certain pharmacy prod
| Recall number | D-1022-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | University Compounding Pharmacy, San Diego, CA, United States |
| Recall initiated | 2013-09-06 |
| Classified | 2013-09-12 |
| Reported by FDA | 2013-09-18 |
| Terminated | 2014-01-21 |
| Distributed | Nationwide (US) |
| Quantity | 70 ml |
| Reason classes | sterility |
| Lot numbers | 513593 |
| Expiration dates | 2013-11-30 |
Product
Testosterone Cypionate/Testosterone Propionate 180-20 mg/mL Injection, 10 mL Vial, University Compounding Pharmacy, 855-398-1800.
Reason for recall
Lack of Assurance of Sterility: University Compounding Pharmacy is voluntarily recalling certain pharmacy products due to lack of assurance of sterility concerns.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1022-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.