FDA Drug recall D-66241-002
SIH-Testosterone Cypionate 200 mg/mL Injectable, 10 mL sterile vial, The Apothecary Shoppe, 6136 E. 51st St. Tulsa, OK 74135
- FDA Drug
- Class II
- terminated
- Published 2013-10-09
On 2013-10-09 the FDA classified a Class II recall of SIH-Testosterone Cypionate 200 mg/mL Injectable, 10 mL sterile vial, The Apothecary Shoppe, 6136 E. 51st St. Tulsa, OK 74135 by Apothecary Shoppe, citing lack of Assurance of Sterility: concerns of sterility assurance with the pharmacy's independent testing laboratory.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-66241-002 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-09-06 |
| Published | 2013-10-09 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Apothecary Shoppe |
| Distribution | OK |
Product
SIH-Testosterone Cypionate 200 mg/mL Injectable, 10 mL sterile vial, The Apothecary Shoppe, 6136 E. 51st St. Tulsa, OK 74135.
Reason
Lack of Assurance of Sterility: concerns of sterility assurance with the pharmacy's independent testing laboratory
Identifiers
| code_info | Lot #s: 05132013@25, Exp 11/9/13; 08072013@4, Exp 2/3/14 |
|---|
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-66241-002%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.