Oscor Inc.
3
Recalls
0
Units Recalled
0
Injuries
0
Deaths
Categories: Medical Device
2026-07-22 to 2026-07-22
| Date | Source | Product | Brand | Severity | Units |
|---|---|---|---|---|---|
| 2026-07-22 | FDA Device | FDA Recall: Abiomed REF: 0052-3025, Introducer Kit for Impella Hemostatic Peel Away Introducer System with Inf | Oscor Inc. | Class I | N/A |
| 2026-07-22 | FDA Device | FDA Recall: Abiomed REF: 0052-3021, Introducer Kit for Impella Hemostatic Peel Away Introducer System with Inf | Oscor Inc. | Class I | N/A |
| 2026-07-22 | FDA Device | FDA Recall: Abiomed REF: 0052-3006, Introducer Kit for Impella Hemostatic Peel Away Introducer System with Inf | Oscor Inc. | Class I | N/A |