Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K102919 |
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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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Venous Hardshell Cardiotomy Reservoir, used during cardiopulmonary bypass Model ... | 2 | 05/30/2023 | Maquet Medical Systems USA |
Venous Hardshell Cardiotomy Reservoir, used during cardiopulmonary bypass Model ... | 2 | 05/26/2023 | Maquet Medical Systems USA |
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