Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K200759 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| NIM Vital Patient Interface 4.0 (P/N: NIM4CPB1) NIM with Software version 1.3.2 | 2 | 06/02/2022 |
FEI # 1045254 Medtronic Xomed, Inc. |
| NIM Vital Nerve Monitoring systems (all serial numbers manufactured) with NIM Vital System versions:... | 1 | 07/24/2024 |
FEI # 1045254 Medtronic Xomed, Inc. |
| NIM Vital Nerve Monitoring System: CONSOLE NIM4CM01 NIM 4.0, REF: NIM4CM01; CONSOLE NIM4CM01RF N... | 2 | 04/18/2025 |
FEI # 1045254 Medtronic Xomed, Inc. |
| NIM Vital Console 4.0 (P/N: NIM4CM01) NIM with Software version 1.3.2 | 2 | 06/02/2022 |
FEI # 1045254 Medtronic Xomed, Inc. |
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