FDA Drug recall D-1341-2015
Chorionic Gonadotropin/ Hydroxocobalamin Lyophilized Powder Injectable, 10,000 UNITS/ 5000 mcg per vial, Rx Only, Manufactured by Park Comp…
- FDA Drug
- Class II
- terminated
- Published 2015-09-09
On 2015-09-09 the FDA classified a Class II recall of Chorionic Gonadotropin/ Hydroxocobalamin Lyophilized Powder Injectable, 10,000 UNITS/ 5000 mcg per vial, Rx Only, Manufactured by Park Comp… by South Coast Specialty Compounding, citing penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1341-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-04-23 |
| Published | 2015-09-09 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | South Coast Specialty Compounding |
| Distribution | US |
Product
Chorionic Gonadotropin/ Hydroxocobalamin Lyophilized Powder Injectable, 10,000 UNITS/ 5000 mcg per vial, Rx Only, Manufactured by Park Compounding, Irving, CA
Reason
Penicillin Cross Contamination: Multiple finished products potentially contaminated with penicillin.
Identifiers
| code_info | Lot # 120322014@1B, Exp 05/15 |
|---|
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-1341-2015%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.