SIH-Testosterone Cypionate 200 mg/mL Injectable — Class II drug recall D-66241-002
Terminated recall by Apothecary Shoppe, reported 2013-10-09, distributed in OK. Lack of Assurance of Sterility: concerns of sterility assurance with the pharmacy's independent testing labora
| Recall number | D-66241-002 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Apothecary Shoppe, Tulsa, OK, United States |
| Recall initiated | 2013-09-06 |
| Classified | 2013-10-03 |
| Reported by FDA | 2013-10-09 |
| Terminated | 2016-02-08 |
| Distributed | OK |
| Quantity | 1,430 ml |
| Reason classes | sterility |
| Expiration dates | 2013-11-09, 2014-02-03 |
Product
SIH-Testosterone Cypionate 200 mg/mL Injectable, 10 mL sterile vial, The Apothecary Shoppe, 6136 E. 51st St. Tulsa, OK 74135.
Reason for recall
Lack of Assurance of Sterility: concerns of sterility assurance with the pharmacy's independent testing laboratory
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-66241-002. 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.