FDA Drug recall D-0021-2024
fentaNYL, 2500 mcg/50 mL, (50 mcg/mL), 50 mL Syringe, Rx only, CAPS, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C…
- FDA Drug
- Class II
- terminated
- Published 2023-10-11
On 2023-10-11 the FDA classified a Class II recall of fentaNYL, 2500 mcg/50 mL, (50 mcg/mL), 50 mL Syringe, Rx only, CAPS, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C… by Central Admixture Pharmacy Services, citing lack of assurance of sterility:.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0021-2024 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2023-09-21 |
| Published | 2023-10-11 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Central Admixture Pharmacy Services |
| Distribution | US |
Product
fentaNYL, 2500 mcg/50 mL, (50 mcg/mL), 50 mL Syringe, Rx only, CAPS, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-2003-3
Reason
Lack of assurance of sterility:
Identifiers
| code_info | Lot:17-275464, Exp. 10/4/2023; 17-275850, Exp. 10/11/2023. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0021-2024%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.