Medical Device Recalls
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Related Medical Device Recalls |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Z-0674-2024 - MYNXGRIP 5F, REF MX5021, Vascular Closure Device (VCD). Used to seal femoral arterial and femoral venous access sites. | 2 | 01/05/2024 |
FEI # 1016427 Cordis US Corp |
| Z-0675-2024 - MYNXGRIP 6F/7F, REF MX6721, Vascular Closure Device (VCD). Used to seal femoral arterial and femoral venous access sites | 2 | 01/05/2024 |
FEI # 1016427 Cordis US Corp |
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