Recalls / Active ingredient / Fosphenytoin Sodium
Fosphenytoin Sodium
4 FDA drug recalls involving the active ingredient “Fosphenytoin Sodium”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2014-05-02 | Class II | Fosphenytoin Sodium Injection, USP, 500 mg PE/10 mL (50 mg PE/mL), (PE= phenytoin sodium equivalents) 10 mL Si | Fresenius Kabi USA, LLC |
| 2014-05-02 | Class II | Fosphenytoin Sodium Injection, USP, 100 mg PE/2 mL (50 mg PE/mL) (PE= phenytoin sodium equivalents) 2 mL Sing | Fresenius Kabi USA, LLC |
| 2012-04-13 | Class II | Fosphenytoin Sodium Injection, USP, 500 mg PE per 10 mL (50 mg PE per mL), 10 mL Single Dose Vial, packaged in | West-ward Pharmaceutical Corp. |
| 2012-04-13 | Class II | Fosphenytoin Sodium Injection, USP, 100 mg PE per 2 mL (50 mg PE per mL), 2 mL Single Dose Vial, packaged in 2 | West-ward Pharmaceutical Corp. |