Teva Pharmaceuticals USA Inc Recall: Alprostadil Injection USP 500 mcg/mL, 1 mL Single Dos
Teva Pharmaceuticals USA Inc Recall: Alprostadil Injection USP 500 mcg/mL, 1 mL Single Dos is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Teva Pharmaceuticals USA Inc; Product: Alprostadil Injection USP 500 mcg/mL, 1 mL Single Dose Vial, 5 vials per Carton, Rx Only, Carton NDC 0703-15
| Recalling firm | Teva Pharmaceuticals USA Inc |
|---|---|
| Product | Alprostadil Injection USP 500 mcg/mL, 1 mL Single Dose Vial, 5 vials per Carton, Rx Only, Carton NDC 0703-1501-02, Distributed by: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054, Vial NDC 0703-1501-01 |
| Reason for recall | Failed Impurities/Degradation Specifications; out-of-specification results for impurities obtained during routine stability testing |
| Classification | Class III (least serious — unlikely to cause adverse health consequences) |
| Status | Terminated |
| Distribution | Product was distributed nationwide in the US Market |
| Recall initiated | 20220518 |
| Recall number | D-0988-2022 |
| Category | drug |
| State | NJ |
| Country | United States |
$29/mo
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