Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K133598 |
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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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Cardiohelp-i Transport Guard with Transport Guard (701072525): is a blood oxygenation and carbon ... | 2 | 04/08/2022 | Maquet Medical Systems USA |
Cardiohelp-i, blood oxygenation and carbon dioxide removal system, Part Numbers 701072780 (Cardiohel... | 2 | 11/09/2023 | Maquet Medical Systems USA |
CARDIOHELP Emergency Drive, Part Numbers 701048002 and 701076205. The CARDIOHELP System is a blood o... | 1 | 12/07/2023 | Maquet Medical Systems USA |
CARDIOHELP-i Heart Lung Support System- A blood oxygenation and carbon dioxide removal system used t... | 2 | 12/14/2023 | Maquet Medical Systems USA |
Venous probe connection cable (REF 701069333 and 701048804) used with the Cardiohelp-i System, part ... | 2 | 12/21/2023 | Maquet Medical Systems USA |
Bubble Sensor (REF: 70105.5720) | 2 | 02/08/2024 | Maquet Medical Systems USA |
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