Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K161361 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Medtronic HawkOne Directional Atherectomy System, Catalog numbers H1-M and H1-M-INT., Multi-vessel, ... | 1 | 01/19/2022 | ev3 Inc. |
Medtronic HawkOne Directional Atherectomy System, Catalog numbers H1-S and H1-S-INT, Small Vessel, 6... | 1 | 01/19/2022 | ev3 Inc. |
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