Testosterone Cypionate Injection — Class II drug recall D-0983-2020
Terminated recall by Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical, reported 2020-03-11, distributed nationwide. Lack of Assurance of Sterility
| Recall number | D-0983-2020 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical, Los Angeles, CA, United States |
| Recall initiated | 2020-01-15 |
| Classified | 2020-03-05 |
| Reported by FDA | 2020-03-11 |
| Terminated | 2023-12-07 |
| Distributed | Nationwide (US) |
| Countries outside the US | BB, DO |
| Reason classes | sterility |
| NDC | 71283-0530-01 |
| Expiration dates | 2020-06-29, 2020-07-06, 2020-08-12, 2020-10-22, 2020-11-10, 2020-11-20, 2020-12-29, 2021-01-16, 2021-01-18 |
Product
Testosterone Cypionate Injection,TESTOSTERONE CYP IN GRAPESEED OIL [10ML] 200 MG/ML INJECTABLE, For IM Use, 10 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0530-1
Reason for recall
Lack of Assurance of Sterility
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-0983-2020. 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.