Medical Device Recalls
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510(K) Number: K122084 |
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| Abiomed REF: 0052-3025, Introducer Kit for Impella Hemostatic Peel Away Introducer System with Inf... | 1 | 07/10/2026 |
FEI # 1035166 Oscor Inc. |
| Abiomed REF: 0052-3021, Introducer Kit for Impella Hemostatic Peel Away Introducer System with Inf... | 1 | 07/10/2026 |
FEI # 1035166 Oscor Inc. |
| Abiomed REF: 0052-3006, Introducer Kit for Impella Hemostatic Peel Away Introducer System with Inf... | 1 | 07/10/2026 |
FEI # 1035166 Oscor Inc. |
| AngioDynamics Safe Sheath Ultralite - Vascular Introducer/Catheter Introducer Catalogue #: VI10 - ... | 2 | 04/21/2021 |
FEI # 3017892510 Angiodynamics Inc. (Navilyst Medical Inc.) |
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