Human Chorionic Gonadotropin Injection — Class II drug recall D-1462-2016
Terminated recall by Talon Compounding Pharmacy, reported 2016-08-31, distributed nationwide. Lack of Assurance of Sterility
| Recall number | D-1462-2016 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Talon Compounding Pharmacy, San Antonio, TX, United States |
| Recall initiated | 2016-07-19 |
| Classified | 2016-08-22 |
| Reported by FDA | 2016-08-31 |
| Terminated | 2017-03-31 |
| Distributed | Nationwide (US) |
| Quantity | 6,500 vials |
| Reason classes | sterility |
Product
Human Chorionic Gonadotropin Injection (a) 2500 iu, (b) 2500 iu with B12, (c) 3500 iu, (d) 5000 iu, (e) 5000 iu with B12, (f) 6000 iu, (g) 7500 iu, (h) 7500 iu with B12, (i)11,000 iu, (j)11,000 iu with B12, (k) 15,000 iu, (l) 20,000 iu, (m) 20,000 iu with B12, 10 mL sterile, depyrogenated vials, Rx Only, Compounded by Talon Compounding Pharmacy, San Antonio, TX 78247
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-1462-2016. 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.