FDA Drug recall D-1342-2015
Methyl Folate Lyophilized Powder for Injection, 20 mg per vial, Rx Only, Manufactured by Park Compounding, Irving, CA
- FDA Drug
- Class II
- terminated
- Published 2015-09-09
On 2015-09-09 the FDA classified a Class II recall of Methyl Folate Lyophilized Powder for Injection, 20 mg per vial, Rx Only, Manufactured by Park Compounding, Irving, CA 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-1342-2015 |
| 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
Methyl Folate Lyophilized Powder for Injection, 20 mg 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 # 11152014@1B, Exp 05/15 Lot # 02082015@3B, Exp 08/14 |
|---|
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-1342-2015%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.