Amneal Pharmaceuticals LLC Recall: Fosphenytoin Sodium Injection, USP, 500 mg PE/10 mL (50
Amneal Pharmaceuticals LLC Recall: Fosphenytoin Sodium Injection, USP, 500 mg PE/10 mL (50 is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Amneal Pharmaceuticals LLC; Product: Fosphenytoin Sodium Injection, USP, 500 mg PE/10 mL (50 mg PE/mL. 10 mL Single Dose Vial, Rx Only. Distributed
| Recalling firm | Amneal Pharmaceuticals LLC |
|---|---|
| Product | Fosphenytoin Sodium Injection, USP, 500 mg PE/10 mL (50 mg PE/mL. 10 mL Single Dose Vial, Rx Only. Distributed by: Amneal Biosciences, Bridgewater, NJ 08807. NDC: 70121-1390-7 |
| Reason for recall | Presence of Particulate Matter |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | MS, NC, OH, TX, UT |
| Recall initiated | 20170831 |
| Recall number | D-0076-2018 |
| Category | drug |
| State | KY |
| Country | United States |
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